{
    "uniprot_canonical_ac": "A4UGR9-1", 
    "ptm_annotation": [], 
    "sequence": {
        "header": "sp|A4UGR9-1|XIRP2_HUMAN Isoform 1 of Xin actin-binding repeat-containing protein 2  OS=Homo sapiens OX=9606 GN=XIRP2 PE=1 SV=2 CANONICAL=A4UGR9-1", 
        "length": 3374, 
        "sequence": "MSPESGHSRIFEATAGPNKPESGFAEDSAARGEGVSDLHEVVSLKERMARYQAAVSRGDCRSFSANMMEESEMCAVPGGLAKVKKQFEDEITSSRNTFAQYQYQHQNRSEQEAIHSSQVGTSRSSQEMARNEQEGSKVQKIDVHGTEMVSHLEKHTEEVNQASQFHQYVQETVIDTPEDEEIPKVSTKLLKEQFEKSAQEKILYSDKEMTTPAKQIKTESEYEETFKPSSVVSTSSTSCVSTSQRKETSTTRYSDHSVTSSTLAQINATSSGMTEEFPPPPPDVLQTSVDVTAFSQSPELPSPPRRLPVPKDVYSKQRNLYELNRLYKHIHPELRKNLEKDYISEVSEIVSSQMNSGSSVSADVQQARYVFENTNDSSQKDLNSEREYLEWDEILKGEVQSIRWIFENQPLDSINNGSPDEGDISRGIADQEIIAGGDVKYTTWMFETQPIDTLGAYSSDTVENAEKIPELARGDVCTARWMFETRPLDSMNKMHQSQEESAVTISKDITGGDVKTVRYMFETQHLDQLGQLHSVDEVHLLQLRSELKEIKGNVKRSIKCFETQPLYVIRDGSGQMLEIKTVHREDVEKGDVRTARWMFETQPLDTINKDITEIKVVRGISMEENVKGGVSKAKWLFETQPLEKIKESEEVIIEKEKIIGTDVSRKCWMFETQPLDILKEVPDADSLQREEIIGGDVQTTKHLFETLPIEALKDSPDIGKLQKITASEEEKGDVRHQKWIFETQPLEDIRKDKKEYTRTVKLEEVDRGDVKNYTHIFESNNLIKFDASHKIEVEGVTRGAVELNKSLFETTPLYAIQDPLGKYHQVKTVQQEEIVRGDVRSCRWLFETRPIDQFDESIHKFQIIRGISAQEIQTGNVKSAKWLFETQPLDSIKYFSDVEETESKTEQTRDIVKGDVKTCKWLFETQPMESLYEKVSLMTSSEEIHKGDVKTCTWLFETQPLDTIKDDSETAVKLQTVKQEEIQGGDVRTACFLFETENLDSIQGEEVKEIKPVEMDIQAGDVSSMRYKFENQSLDSISSSSEEVLKKIKTLKTEDIQKGNVLNCRWLFENQPIDKIKESQEGDECVKTVTDIQGGDVRKGCFIFETFSLDEIKEESDYISTKKTITEEVIQGDVKSYRMLFETQPLYAIQDREGSYHEVTTVKKEEVIHGDVRGTRWLFETKPLDSINKSETVYVIKSVTQEDIQKGDVSSVRYRFETQPLDQISEESHNIMPSIDHIQGGNVKTSRQFFESENFDKNNYIRTVSVNEIQKGNVKTSTWLFETHTMDELRGEGLEYENIKTVTQEDVQKGDVKQAVWLFENRTFDSIMEAHKGITKMTKEEIPPSDVKTTTWLFETTPLHEFNETRVEKIEIIGKSIKETLEDLYSQKVIQAPGIIIEADEIGDVRMAKYKLMNQASPEIQKEEIIRADLRNIMVNLLSKRDCTEREILISEEEKGNVNLTKTQLLNRSTEFHAEKEEIVKGDVQQAIKNLFSEERSVKKGILIQEDEKGDINMTIYCLLHENDGDTIEREEVIGGDVKRTIHNLLSSTSNNKISERAKIDASERGNVQFFTTCIEAGALDYLKQLHTESNETLTAKKQEGEKEIIGGDVEGTKLLLKKRQSLVERTVSETDIIPGDVHNTVKVFMTEPQSTFGKIPKEEIIKGDLTSTLNSLSQAVNQKTVTKTEEIIKGNMLATLKSLKESSHRWKESKQPDAIPGDIEKAIECLEKATNTKTEILKKELLKDDLETSLRSLKEAQRSFKEVHKEGVIKKDAKAVMAGSSGEQKTDIHQVAVQRNKNSLLQPKPGPFEPAAKWQGGADTLSQTMGKSCHGNLVEERTEVNLPKAPKGTVKIVIDREQNNDALEKSLRRLSNSHHKSNVLESGDKTGVWTDTTGEQHLRDEYMSRQLTSTVSVKNNLTTKESDRAVRELKKDDVFNSIQSAGKTVGKQQTYELRNDHQKMEGFHIKSPKKTKNIKILTDTQSSKPSPTQHPVSMPVGGTYDLSGDFQKQTLLKQETKYSNKDIKKKNINLQPMWQLLPVEQDTSNVTEMKVSEKSHNTFKATNKKRETDVHLKSQDFLMKTNTSTGLKMAMERSLNPINFNPENNVKESECPLPPPSPPPPPPSNASSEIEFPLPPPPPLMMFPEKNGFLPSLSTEKIKAEFESFPGLPLPPPPVDEKSERESSSMFLPPPPPPTPSQKPAHLLSSSAPEKHSGDFMQQYSQKEASNSQNSQAKIITGKTGVLPPPTLPKPKLPKHIKDNKNDFSPKVELATSLSDMECKITTSKDQKKVMVMTSSEHTETKQNVISKSLDERKQLSIDSANCLSHTVPGTSAPRKKQIAPLIKSHSFPESSGQQNPKPYMRKFKTPLMIAEEKYRQQKEEIEKQKQESSYYNIVKTQSQNQHITEVEKEMPLQKTNEEVSLSGIDSECTVVQPSPGSQSNARILGVCSDNQLSTTSPETVAAKRLHHVLAASEDKDKMKKEVLQSSRDIMQSKSACEIKQSHQECSTQQTQQKKYLEQLHLPQSKPISPNFKVKTIKLPTLDHTLNETDHSYESHKQQSEIDVQTFTKKQYLKTKKTEASTECSHKQSLAERHYQLPKKEKRVTVQLPTESIQKNQEDKLKMVPRKQREFSGSDRGKLPGSEEKNQGPSMIGRKEERLITERKHEHLKNKSAPKVVKQKVIDAHLDSQTQNFQQTQIQTAESKAEHKKLPQPYNSLQEEKCLEVKGIQEKQVFSNTKDSKQEITQNKSFFSSVKESQRDDGKGALNIVEFLRKREELQQILSRVKQFEAEPNKSGLKTFQTLLNTIPGWLISEDKREYAVHIAMENNLEKVKEEITHIKTQAEDMLVSYENIIQTAMMSSKTGKPGNKPTSLDETSSKVSNVHVSNNKNSEQKENKIAKEKTVQHQVAAHHEATVRSHVKTHQEIKLDDSNIPPPSLKTRPPSPTFITIESTARRTENPTKNELSQSPKKDSYVEPPPRRPMSQKSEIHRANTSPSPPRSRSEQLVRLKDTTAKLSKGAIPCPAATPVPIVEKRSEIIMSPATLRRQIKIETRGRDSPPTITIPVNINHAASGSFRESVDAQEEIRKVEKRATYVHKDGLNSTDHMVPDTESYDAVEIIRKVAVPPRLSEHTQRYEAANRTVQMAENFVNDPENEINRWFREFEHGPVSEAKSNRRVYAKGETNHNIQQESRTFCKEEFGLTSLGNTSFTDFSCKHPRELREKIPVKQPRICSETRSLSEHFSGMDAFESQIVESKMKTSSSHSSEAGKSGCDFKHAPPTYEDVIAGHILDISDSPKEVRKNFQKTWQESGRVFKGLGYATADASATEMRTTFQEESAFISEAAAPRQGNMYTLSKDSLSNGVPSGRQAEFS"
    }, 
    "uniprot_id": "", 
    "enzyme_annotation": [], 
    "glycation": [], 
    "keywords": [
        "glycoprotein", 
        "reported_with_glycan.oglcnac_db", 
        "reported_with_glycan.glygen_ds"
    ], 
    "species": [
        {
            "common_name": "Human", 
            "evidence": [
                {
                    "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                    "id": "A4UGR9", 
                    "database": "UniProtKB"
                }
            ], 
            "name": "Homo sapiens", 
            "taxid": 9606
        }
    ], 
    "go_annotation": {
        "categories": [
            {
                "go_terms": [
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051015", 
                        "pmid": "15454575", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                                "id": "A4UGR9", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "actin filament binding", 
                        "id": "GO:0051015"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051393", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                                "id": "A4UGR9", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "alpha-actinin binding", 
                        "id": "GO:0051393"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003779", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                                "id": "A4UGR9", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "actin binding", 
                        "id": "GO:0003779"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                                "id": "A4UGR9", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "metal ion binding", 
                        "id": "GO:0046872"
                    }
                ], 
                "total": 4, 
                "name": "Molecular Function"
            }, 
            {
                "go_terms": [
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030054", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                                "id": "A4UGR9", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "cell junction", 
                        "id": "GO:0030054"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030018", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                                "id": "A4UGR9", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "Z disc", 
                        "id": "GO:0030018"
                    }
                ], 
                "total": 2, 
                "name": "Cellular Component"
            }, 
            {
                "go_terms": [
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030036", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                                "id": "A4UGR9", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "actin cytoskeleton organization", 
                        "id": "GO:0030036"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055008", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                                "id": "A4UGR9", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "cardiac muscle tissue morphogenesis", 
                        "id": "GO:0055008"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003281", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                                "id": "A4UGR9", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "ventricular septum development", 
                        "id": "GO:0003281"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045216", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                                "id": "A4UGR9", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "cell-cell junction organization", 
                        "id": "GO:0045216"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007507", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                                "id": "A4UGR9", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "heart development", 
                        "id": "GO:0007507"
                    }
                ], 
                "total": 5, 
                "name": "Biological Process"
            }
        ]
    }, 
    "publication": [
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/12203715", 
                    "type": "PubMed", 
                    "id": "12203715"
                }
            ], 
            "title": "Localization of the novel Xin protein to the adherens junction complex in cardiac and skeletal muscle during development.", 
            "journal": "Developmental dynamics : an official publication of the American Association of Anatomists", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Sinn HW, Balsamo J, Lilien J, Lin JJ", 
            "date": "2002"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/14687087", 
                    "type": "PubMed", 
                    "id": "14687087"
                }
            ], 
            "title": "Sequencing, tissue distribution and physical mapping of the porcine homologue of cardiomyopathy associated 3 (CMYA3).", 
            "journal": "Animal genetics", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Pan PW, Li K, Tuggle CK, Yu M, Liu B, Zhao SH", 
            "date": "2003"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/15454575", 
                    "type": "PubMed", 
                    "id": "15454575"
                }
            ], 
            "title": "Xin repeats define a novel actin-binding motif.", 
            "journal": "J. Cell Sci.", 
            "evidence": [
                {
                    "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                    "id": "A4UGR9", 
                    "database": "UniProtKB"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Rottner K., Fuerst D.O., Vakeel P., van der Ven P.F.M., Himmel M., Loewe T., Pacholsky D., Stradal T.", 
            "date": "2004"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/16205742", 
                    "type": "PubMed", 
                    "id": "16205742"
                }
            ], 
            "title": "SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample.", 
            "journal": "European journal of human genetics : EJHG", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Blasi F, Bacchelli E, Carone S, Toma C, Monaco AP, Bailey AJ, Maestrini E", 
            "date": "2006"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/17046827", 
                    "type": "PubMed", 
                    "id": "17046827"
                }
            ], 
            "title": "Myomaxin is a novel transcriptional target of MEF2A that encodes a Xin-related alpha-actinin-interacting protein.", 
            "journal": "The Journal of biological chemistry", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Huang HT, Brand OM, Mathew M, Ignatiou C, Ewen EP, McCalmon SA, Naya FJ", 
            "date": "2006"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/20520587", 
                    "type": "PubMed", 
                    "id": "20520587"
                }
            ], 
            "title": "Genome-wide association study identifies genes that may contribute to risk for developing heroin addiction.", 
            "journal": "Psychiatric genetics", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Nielsen DA, Ji F, Yuferov V, Ho A, He C, Ott J, Kreek MJ", 
            "date": "2010"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/24475916", 
                    "type": "PubMed", 
                    "id": "24475916"
                }
            ], 
            "title": "CCDD Phenotype Associated with a Small Chromosome 2 Deletion.", 
            "journal": "Seminars in ophthalmology", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Abu-Amero KK, Bosley TM, Kondkar AA, Oystreck DT, Khan AO", 
            "date": "2015"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/25865352", 
                    "type": "PubMed", 
                    "id": "25865352"
                }
            ], 
            "title": "A genome-wide association study reveals 2 new susceptibility loci for atopic dermatitis.", 
            "journal": "The Journal of allergy and clinical immunology", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Schaarschmidt H, Ellinghaus D, Rodriguez E, Kretschmer A, Baurecht H, Lipinski S, Meyer-Hoffert U, Harder J, Lieb W, Novak N, Folster-Holst R, Esparza-Gordillo J, Marenholz I, Ruschendorf F, Hubner N, Reischl E, Waldenberger M, Gieger C, Illig T, Kabesch M, Zhang XJ, Xiao FL, Lee YA, Franke A, Weidinger S", 
            "date": "2015"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/26566883", 
                    "type": "PubMed", 
                    "id": "26566883"
                }
            ], 
            "title": "Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family.", 
            "journal": "J. Med. Genet.", 
            "evidence": [
                {
                    "url": "https://www.uniprot.org/uniprot/A4UGR9", 
                    "id": "A4UGR9", 
                    "database": "UniProtKB"
                }
            ], 
            "authors": "Wiemann S., Rappold G.A., Wade R.C., Aslamkhan M., Berkel S., Mustafa G., Paramasivam N., Rafiullah R., Schlesner M., Thiel C.", 
            "date": "2016"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/28411811", 
                    "type": "PubMed", 
                    "id": "28411811"
                }
            ], 
            "title": "A novel strategy for global mapping of O-GlcNAc proteins and peptides using selective enzymatic deglycosylation, HILIC enrichment and mass spectrometry identification.", 
            "journal": "Talanta", 
            "evidence": [
                {
                    "url": "https://data.glygen.org/GLYDS000517", 
                    "id": "GLYDS000517", 
                    "database": "GlyGen"
                }
            ], 
            "authors": "Shen B, Zhang W, Shi Z, Tian F, Deng Y, Sun C, Wang G, Qin W, Qian X", 
            "date": "2017"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/29306897", 
                    "type": "PubMed", 
                    "id": "29306897"
                }
            ], 
            "title": "Critical Roles of Xirp Proteins in Cardiac Conduction and Their Rare Variants Identified in Sudden Unexplained Nocturnal Death Syndrome and Brugada Syndrome in Chinese Han Population.", 
            "journal": "Journal of the American Heart Association", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Huang L, Wu KH, Zhang L, Wang Q, Tang S, Wu Q, Jiang PH, Lin JJ, Guo J, Wang L, Loh SH, Cheng J", 
            "date": "2018"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/29351928", 
                    "type": "PubMed", 
                    "id": "29351928"
                }
            ], 
            "title": "Mapping and Quantification of Over 2000 O-linked Glycopeptides in Activated Human T Cells with Isotope-Targeted Glycoproteomics (Isotag).", 
            "journal": "Molecular & cellular proteomics : MCP", 
            "evidence": [
                {
                    "url": "https://data.glygen.org/GLYDS000517", 
                    "id": "GLYDS000517", 
                    "database": "GlyGen"
                }, 
                {
                    "url": "https://data.glygen.org/GLYDS000142", 
                    "id": "GLYDS000142", 
                    "database": "GlyGen"
                }
            ], 
            "authors": "Woo CM, Lund PJ, Huang AC, Davis MM, Bertozzi CR, Pitteri SJ", 
            "date": "2018"
        }
    ], 
    "uniprot_ac": "A4UGR9", 
    "gene_names": [
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/A4UGR9", 
            "type": "synonym", 
            "resource": "RefSeq", 
            "name": "CMYA3"
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9", 
            "type": "synonym", 
            "resource": "UniProtKB", 
            "name": "CMYA3"
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/A4UGR9", 
            "type": "synonym", 
            "resource": "RefSeq", 
            "name": "XIRP2"
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9", 
            "type": "recommended", 
            "resource": "UniProtKB", 
            "name": "XIRP2"
        }
    ], 
    "reactions": [], 
    "isoforms": [
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9#A0A0A0MQZ3-1", 
            "isoform_ac": "A0A0A0MQZ3-1", 
            "locus": {
                "end_pos": 167249151, 
                "strand": "-", 
                "start_pos": 167254123, 
                "chromosome": "2", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENST00000295237", 
                        "id": "ENST00000295237", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSP00000295237", 
                        "id": "ENSP00000295237", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "tr|A0A0A0MQZ3-1|A0A0A0MQZ3_HUMAN Computationally mapped isoform of Xin actin-binding repeat-containing protein 2  OS=Homo sapiens OX=9606 GN=XIRP2 PE=1 SV=1 CANONICAL=A4UGR9-1", 
                "length": 963, 
                "sequence": "MPLQKTNEEVSLSGIDSECTVVQPSPGSQSNARILGVCSDNQLSTTSPETVAAKRLHHVLAASEDKDKMKKEVLQSSRDIMQSKSACEIKQSHQECSTQQTQQKKYLEQLHLPQSKPISPNFKVKTIKLPTLDHTLNETDHSYESHKQQSEIDVQTFTKKQYLKTKKTEASTECSHKQSLAERHYQLPKKEKRVTVQLPTESIQKNQEDKLKMVPRKQREFSGSDRGKLPGSEEKNQGPSMIGRKEERLITERKHEHLKNKSAPKVVKQKVIDAHLDSQTQNFQQTQIQTAESKAEHKKLPQPYNSLQEEKCLEVKGIQEKQVFSNTKDSKQEITQNKSFFSSVKESQRDDGKGALNIVEFLRKREELQQILSRVKQFEAEPNKSGLKTFQTLLNTIPGWLISEDKREYAVHIAMENNLEKVKEEITHIKTQAEDMLVSYENIIQTAMMSSKTGKPGNKPTSLDETSSKVSNVHVSNNKNSEQKENKIAKEKTVQHQVAAHHEATVRSHVKTHQEIKLDDSNIPPPSLKTRPPSPTFITIESTARRTENPTKNELSQSPKKDSYVEPPPRRPMSQKSEIHRANTSPSPPRSRSEQLVRLKDTTAKLSKGAIPCPAATPVPIVEKRSEIIMSPATLRRQIKIETRGRDSPPTITIPVNINHAASGSFRESVDAQEEIRKVEKRATYVHKDGLNSTDHMVPDTESYDAVEIIRKVAVPPRLSEHTQRYEAANRTVQMAENFVNDPENEINRWFREFEHGPVSEAKSNRRVYAKGETNHNIQQESRTFCKEEFGLTSLGNTSFTDFSCKHPRELREKIPVKQPRICSETRSLSEHFSGMDAFESQIVESKMKTSSSHSSEAGKSGCDFKHAPPTYEDVIAGHILDISDSPKEVRKNFQKTWQESGRVFKGLGYATADASATEMRTTFQEESAFISEAAAPRQGNMYTLSKDSLSNGVPSGRQAEFS"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9#A0A5F9ZH43-1", 
            "isoform_ac": "A0A5F9ZH43-1", 
            "locus": {
                "end_pos": 167210839, 
                "strand": "-", 
                "start_pos": 167259360, 
                "chromosome": "2", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENST00000672671", 
                        "id": "ENST00000672671", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSP00000499978", 
                        "id": "ENSP00000499978", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "tr|A0A5F9ZH43-1|A0A5F9ZH43_HUMAN Computationally mapped isoform of Xin actin-binding repeat-containing protein 2  OS=Homo sapiens OX=9606 GN=XIRP2 PE=1 SV=1 CANONICAL=A4UGR9-1", 
                "length": 3837, 
                "sequence": "MARYQAAVSRGDCRSFSANMMEESEMCAVPGGLAKVKKQFEDEITSSRNTFAQYQYQHQNRSEQEAIHSSQVGTSRSSQEMARNEQEGSKVQKIDVHGTEMVSHLEKHTEEVNQASQFHQYVQETVIDTPEDEEIPKVSTKLLKEQFEKSAQEKILYSDKEMTTPAKQIKTESEYEETFKPSSVVSTSSTSCVSTSQRKETSTTRYSDHSVTSSTLAQINATSSGMTEEFPPPPPDVLQTSVDVTAFSQSPELPSPPRRLPVPKDVYSKQRNLYELNRLYKHIHPELRKNLEKDYISEVSEIVSSQMNSGSSVSADVQQARYVFENTNDSSQKDLNSEREYLEWDEILKGEVQSIRWIFENQPLDSINNGSPDEGDISRGIADQEIIAGGDVKYTTWMFETQPIDTLGAYSSDTVENAEKIPELARGDVCTARWMFETRPLDSMNKMHQSQEESAVTISKDITGGDVKTVRYMFETQHLDQLGQLHSVDEVHLLQLRSELKEIKGNVKRSIKCFETQPLYVIRDGSGQMLEIKTVHREDVEKGDVRTARWMFETQPLDTINKDITEIKVVRGISMEENVKGGVSKAKWLFETQPLEKIKESEEVIIEKEKIIGTDVSRKCWMFETQPLDILKEVPDADSLQREEIIGGDVQTTKHLFETLPIEALKDSPDIGKLQKITASEEEKGDVRHQKWIFETQPLEDIRKDKKEYTRTVKLEEVDRGDVKNYTHIFESNNLIKFDASHKIEVEGVTRGAVELNKSLFETTPLYAIQDPLGKYHQVKTVQQEEIVRGDVRSCRWLFETRPIDQFDESIHKFQIIRGISAQEIQTGNVKSAKWLFETQPLDSIKYFSDVEETESKTEQTRDIVKGDVKTCKWLFETQPMESLYEKVSLMTSSEEIHKGDVKTCTWLFETQPLDTIKDDSETAVKLQTVKQEEIQGGDVRTACFLFETENLDSIQGEEVKEIKPVEMDIQAGDVSSMRYKFENQSLDSISSSSEEVLKKIKTLKTEDIQKGNVLNCRWLFENQPIDKIKESQEGDECVKTVTDIQGGDVRKGCFIFETFSLDEIKEESDYISTKKTITEEVIQGDVKSYRMLFETQPLYAIQDREGSYHEVTTVKKEEVIHGDVRGTRWLFETKPLDSINKSETVYVIKSVTQEDIQKGDVSSVRYRFETQPLDQISEESHNIMPSIDHIQGGNVKTSRQFFESENFDKNNYIRTVSVNEIQKGNVKTSTWLFETHTMDELRGEGLEYENIKTVTQEDVQKGDVKQAVWLFENRTFDSIMEAHKGITKMTKEEIPPSDVKTTTWLFETTPLHEFNETRVEKIEIIGKSIKETLEDLYSQKVIQAPGIIIEADEIGDVRMAKYKLMNQASPEIQKEEIIRADLRNIMVNLLSKRDCTEREILISEEEKGNVNLTKTQLLNRSTEFHAEKEEIVKGDVQQAIKNLFSEERSVKKGILIQEDEKGDINMTIYCLLHENDGDTIEREEVIGGDVKRTIHNLLSSTSNNKISERAKIDASERGNVQFFTTCIEAGALDYLKQLHTESNETLTAKKQEGEKEIIGGDVEGTKLLLKKRQSLVERTVSETDIIPGDVHNTVKVFMTEPQSTFGKIPKEEIIKGDLTSTLNSLSQAVNQKTVTKTEEIIKGNMLATLKSLKESSHRWKESKQPDAIPGDIEKAIECLEKATNTKTEILKKELLKDDLETSLRSLKEAQRSFKEVHKEGVIKKDAKAVMAGSSGEQKTDIHQVAVQRNKNSLLQPKPGPFEPAAKWQGGADTLSQTMGKSCHGNLVEERTEVNLPKAPKGTVKIVIDREQNNDALEKSLRRLSNSHHKSNVLESGDKTGVWTDTTGEQHLRDEYMSRQLTSTVSVKNNLTTKESDRAVRELKKDDVFNSIQSAGKTVGKQQTYELRNDHQKMEGFHIKSPKKTKNIKILTDTQSSKPSPTQHPVSMPVGGTYDLSGDFQKQTLLKQETKYSNKDIKKKNINLQPMWQLLPVEQDTSNVTEMKVSEKSHNTFKATNKKRETDVHLKSQDFLMKTNTSTGLKMAMERSLNPINFNPENNVKESECPLPPPSPPPPPPSNASSEIEFPLPPPPPLMMFPEKNGFLPSLSTEKIKAEFESFPGLPLPPPPVDEKSERESSSMFLPPPPPPTPSQKPAHLLSSSAPEKHSGDFMQQYSQKEASNSQNSQAKIITGKTGVLPPPTLPKPKLPKHIKDNKNDFSPKVELATSLSDMECKITTSKDQKKVMVMTSSEHTETKQNVISKSLDERKQLSIDSANCLSHTVPGTSAPRKKQIAPLIKSHSFPESSGQQNPKPYMRKFKTPLMIAEEKYRQQKEEIEKQKQESSYYNIVKTQSQNQHITEVEKEMPLQKTNEEVSLSGIDSECTVVQPSPGSQSNARILGVCSDNQLSTTSPETVAAKRLHHVLAASEDKDKMKKEVLQSSRDIMQSKSACEIKQSHQECSTQQTQQKKYLEQLHLPQSKPISPNFKVKTIKLPTLDHTLNETDHSYESHKQQSEIDVQTFTKKQYLKTKKTEASTECSHKQSLAERHYQLPKKEKRVTVQLPTESIQKNQEDKLKMVPRKQREFSGSDRGKLPGSEEKNQGPSMIGRKEERLITERKHEHLKNKSAPKVVKQKVIDAHLDSQTQNFQQTQIQTAESKAEHKKLPQPYNSLQEEKCLEVKGIQEKQVFSNTKDSKQEITQNKSFFSSVKESQRDDGKGALNIVEFLRKREELQQILSRVKQFEAEPNKSGLKTFQTLLNTIPGWLISEDKREYAVHIAMENNLEKVKEEITHIKTQAEDMLVSYENIIQTAMMSSKTGKPGNKPTSLDETSSKVSNVHVSNNKNSEQKENKIAKEKTVQHQVAAHHEATVRSHVKTHQEIKLDDSNIPPPSLKTRPPSPTFITIESTARRTENPTKNELSQSPKKDSYVEPPPRRPMSQKSEIHRANTSPSPPRSRSEQLVRLKDTTAKLSKGAIPCPAATPVPIVEKRSEIIMSPATLRRQIKIETRGRDSPPTITIPVNINHAASGSFRESVDAQEEIRKVEKRATYVHKDGLNSTDHMVPDTESYDAVEIIRKVAVPPRLSEHTQRYEAANRTVQMAENFVNDPENEINRWFREFEHGPVSEAKSNRRVYAKGETNHNIQQESRTFCKEEFGLTSLGNTSFTDFSCKHPRELREKIPVKQPRICSETRSLSEHFSGMDAFESQIVESKMKTSSSHSSEAGKSGCDFKHAPPTYEDVIAGHILDISDSPKEVRKNFQKTWQESGRVFKGLGYATADASATEMRTTFQEESAFISDKEICILCQKTVYPMECLVADKQNFHKSCFRCHHCNSKLSLGNYASLHGQIYCKPHFKQLFKSKGNYDEGFGHKQHKDRWNCKNQSRSVDFIPNEEPNMCKNIAENTLVPGDRNEHLDAGNSEGQRNDLRKLGERGKLKVIWPPSKEIPKKTLPFEEELKMSKPKWPPEMTTLLSPEFKSESLLEDVRTPENKGQRQDHFPFLQPYLQSTHVCQKEDVIGIKEMKMPEGRKDEKKEGRKNVQDRPSEAEDTKSNRKSAMDLNDNNNVIVQSAEKEKNEKTNQTNGAEVLQVTNTDDEMMPENHKENLNKNNNNNYVAVSYLNNCRQKTSILEFLDLLPLSSEANDTANEYEIEKLENTSRISELLGIFESEKTYSRNVLAMALKKQTDRAAAGSPVQPAPKPSLSRGLMVKGGSSIISPDTNLLNIKGSHSKSKNLHFFFSNTVKITAFSKKNENIFNCDLIDSVDQIKNMPCLDLREFGKDVKPWHVETTEAARNNENTGFDALSHECTAKPLFPRVEVQSEQLTVEEQIKRNRCYSDTE"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9#A0A5F9ZHW6-1", 
            "isoform_ac": "A0A5F9ZHW6-1", 
            "locus": {
                "end_pos": 166891190, 
                "strand": "-", 
                "start_pos": 167259360, 
                "chromosome": "2", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENST00000672716", 
                        "id": "ENST00000672716", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSP00000500725", 
                        "id": "ENSP00000500725", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "tr|A0A5F9ZHW6-1|A0A5F9ZHW6_HUMAN Computationally mapped isoform of Xin actin-binding repeat-containing protein 2  OS=Homo sapiens OX=9606 GN=XIRP2 PE=1 SV=1 CANONICAL=A4UGR9-1", 
                "length": 946, 
                "sequence": "MADNLDPSMFPMQKGSLNLLRQKWESCDYQRSECHPRDSHCTIFQPQESKLLAPEGEVVSAPQSLDPTSLPYSTGEEMWSSKPEEKDSVDKSNNTREYGRPEVLKEDSLSSRRRIERFSIALDELRSVFEAPKSGNKPAEYGGKEVEIERSLCSPAFKSHPGSQLEDSVKDSDKKGKETSFDKMSPESGHSRIFEATAGPNKPESGFAEDSAARGEGVSDLHEVVSLKERMARYQAAVSRGDCRSFSANMMEESEMCAVPGGLAKVKKQFEDEITSSRNTFAQYQYQHQNRSEQEAIHSSQVGTSRSSQEMARNEQEGSKVQKIDVHGTEMVSHLEKHTEEVNQASQFHQYVQETVIDTPEDEEIPKVSTKLLKEQFEKSAQEKILYSDKEMTTPAKQIKKLLLQDKEICILCQKTVYPMECLVADKQNFHKSCFRCHHCNSKLSLGNYASLHGQIYCKPHFKQLFKSKGNYDEGFGHKQHKDRWNCKNQSRSVDFIPNEEPNMCKNIAENTLVPGDRNEHLDAGNSEGQRNDLRKLGERGKLKVIWPPSKEIPKKTLPFEEELKMSKPKWPPEMTTLLSPEFKSESLLEDVRTPENKGQRQDHFPFLQPYLQSTHVCQKEDVIGIKEMKMPEGRKDEKKEGRKNVQDRPSEAEDTKSNRKSAMDLNDNNNVIVQSAEKEKNEKTNQTNGAEVLQVTNTDDEMMPENHKENLNKNNNNNYVAVSYLNNCRQKTSILEFLDLLPLSSEANDTANEYEIEKLENTSRISELLGIFESEKTYSRNVLAMALKKQTDRAAAGSPVQPAPKPSLSRGLMVKGGSSIISPDTNLLNIKGSHSKSKNLHFFFSNTVKITAFSKKNENIFNCDLIDSVDQIKNMPCLDLREFGKDVKPWHVETTEAARNNENTGFDALSHECTAKPLFPRVEVQSEQLTVEEQIKRNRCYSDTE"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9#A4UGR9-1", 
            "isoform_ac": "A4UGR9-1", 
            "locus": {
                "end_pos": 167136026, 
                "strand": "-", 
                "start_pos": 167254123, 
                "chromosome": "2", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENST00000628543", 
                        "id": "ENST00000628543", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSP00000486198", 
                        "id": "ENSP00000486198", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "sp|A4UGR9-1|XIRP2_HUMAN Isoform 1 of Xin actin-binding repeat-containing protein 2  OS=Homo sapiens OX=9606 GN=XIRP2 PE=1 SV=2 CANONICAL=A4UGR9-1", 
                "length": 3374, 
                "sequence": "MSPESGHSRIFEATAGPNKPESGFAEDSAARGEGVSDLHEVVSLKERMARYQAAVSRGDCRSFSANMMEESEMCAVPGGLAKVKKQFEDEITSSRNTFAQYQYQHQNRSEQEAIHSSQVGTSRSSQEMARNEQEGSKVQKIDVHGTEMVSHLEKHTEEVNQASQFHQYVQETVIDTPEDEEIPKVSTKLLKEQFEKSAQEKILYSDKEMTTPAKQIKTESEYEETFKPSSVVSTSSTSCVSTSQRKETSTTRYSDHSVTSSTLAQINATSSGMTEEFPPPPPDVLQTSVDVTAFSQSPELPSPPRRLPVPKDVYSKQRNLYELNRLYKHIHPELRKNLEKDYISEVSEIVSSQMNSGSSVSADVQQARYVFENTNDSSQKDLNSEREYLEWDEILKGEVQSIRWIFENQPLDSINNGSPDEGDISRGIADQEIIAGGDVKYTTWMFETQPIDTLGAYSSDTVENAEKIPELARGDVCTARWMFETRPLDSMNKMHQSQEESAVTISKDITGGDVKTVRYMFETQHLDQLGQLHSVDEVHLLQLRSELKEIKGNVKRSIKCFETQPLYVIRDGSGQMLEIKTVHREDVEKGDVRTARWMFETQPLDTINKDITEIKVVRGISMEENVKGGVSKAKWLFETQPLEKIKESEEVIIEKEKIIGTDVSRKCWMFETQPLDILKEVPDADSLQREEIIGGDVQTTKHLFETLPIEALKDSPDIGKLQKITASEEEKGDVRHQKWIFETQPLEDIRKDKKEYTRTVKLEEVDRGDVKNYTHIFESNNLIKFDASHKIEVEGVTRGAVELNKSLFETTPLYAIQDPLGKYHQVKTVQQEEIVRGDVRSCRWLFETRPIDQFDESIHKFQIIRGISAQEIQTGNVKSAKWLFETQPLDSIKYFSDVEETESKTEQTRDIVKGDVKTCKWLFETQPMESLYEKVSLMTSSEEIHKGDVKTCTWLFETQPLDTIKDDSETAVKLQTVKQEEIQGGDVRTACFLFETENLDSIQGEEVKEIKPVEMDIQAGDVSSMRYKFENQSLDSISSSSEEVLKKIKTLKTEDIQKGNVLNCRWLFENQPIDKIKESQEGDECVKTVTDIQGGDVRKGCFIFETFSLDEIKEESDYISTKKTITEEVIQGDVKSYRMLFETQPLYAIQDREGSYHEVTTVKKEEVIHGDVRGTRWLFETKPLDSINKSETVYVIKSVTQEDIQKGDVSSVRYRFETQPLDQISEESHNIMPSIDHIQGGNVKTSRQFFESENFDKNNYIRTVSVNEIQKGNVKTSTWLFETHTMDELRGEGLEYENIKTVTQEDVQKGDVKQAVWLFENRTFDSIMEAHKGITKMTKEEIPPSDVKTTTWLFETTPLHEFNETRVEKIEIIGKSIKETLEDLYSQKVIQAPGIIIEADEIGDVRMAKYKLMNQASPEIQKEEIIRADLRNIMVNLLSKRDCTEREILISEEEKGNVNLTKTQLLNRSTEFHAEKEEIVKGDVQQAIKNLFSEERSVKKGILIQEDEKGDINMTIYCLLHENDGDTIEREEVIGGDVKRTIHNLLSSTSNNKISERAKIDASERGNVQFFTTCIEAGALDYLKQLHTESNETLTAKKQEGEKEIIGGDVEGTKLLLKKRQSLVERTVSETDIIPGDVHNTVKVFMTEPQSTFGKIPKEEIIKGDLTSTLNSLSQAVNQKTVTKTEEIIKGNMLATLKSLKESSHRWKESKQPDAIPGDIEKAIECLEKATNTKTEILKKELLKDDLETSLRSLKEAQRSFKEVHKEGVIKKDAKAVMAGSSGEQKTDIHQVAVQRNKNSLLQPKPGPFEPAAKWQGGADTLSQTMGKSCHGNLVEERTEVNLPKAPKGTVKIVIDREQNNDALEKSLRRLSNSHHKSNVLESGDKTGVWTDTTGEQHLRDEYMSRQLTSTVSVKNNLTTKESDRAVRELKKDDVFNSIQSAGKTVGKQQTYELRNDHQKMEGFHIKSPKKTKNIKILTDTQSSKPSPTQHPVSMPVGGTYDLSGDFQKQTLLKQETKYSNKDIKKKNINLQPMWQLLPVEQDTSNVTEMKVSEKSHNTFKATNKKRETDVHLKSQDFLMKTNTSTGLKMAMERSLNPINFNPENNVKESECPLPPPSPPPPPPSNASSEIEFPLPPPPPLMMFPEKNGFLPSLSTEKIKAEFESFPGLPLPPPPVDEKSERESSSMFLPPPPPPTPSQKPAHLLSSSAPEKHSGDFMQQYSQKEASNSQNSQAKIITGKTGVLPPPTLPKPKLPKHIKDNKNDFSPKVELATSLSDMECKITTSKDQKKVMVMTSSEHTETKQNVISKSLDERKQLSIDSANCLSHTVPGTSAPRKKQIAPLIKSHSFPESSGQQNPKPYMRKFKTPLMIAEEKYRQQKEEIEKQKQESSYYNIVKTQSQNQHITEVEKEMPLQKTNEEVSLSGIDSECTVVQPSPGSQSNARILGVCSDNQLSTTSPETVAAKRLHHVLAASEDKDKMKKEVLQSSRDIMQSKSACEIKQSHQECSTQQTQQKKYLEQLHLPQSKPISPNFKVKTIKLPTLDHTLNETDHSYESHKQQSEIDVQTFTKKQYLKTKKTEASTECSHKQSLAERHYQLPKKEKRVTVQLPTESIQKNQEDKLKMVPRKQREFSGSDRGKLPGSEEKNQGPSMIGRKEERLITERKHEHLKNKSAPKVVKQKVIDAHLDSQTQNFQQTQIQTAESKAEHKKLPQPYNSLQEEKCLEVKGIQEKQVFSNTKDSKQEITQNKSFFSSVKESQRDDGKGALNIVEFLRKREELQQILSRVKQFEAEPNKSGLKTFQTLLNTIPGWLISEDKREYAVHIAMENNLEKVKEEITHIKTQAEDMLVSYENIIQTAMMSSKTGKPGNKPTSLDETSSKVSNVHVSNNKNSEQKENKIAKEKTVQHQVAAHHEATVRSHVKTHQEIKLDDSNIPPPSLKTRPPSPTFITIESTARRTENPTKNELSQSPKKDSYVEPPPRRPMSQKSEIHRANTSPSPPRSRSEQLVRLKDTTAKLSKGAIPCPAATPVPIVEKRSEIIMSPATLRRQIKIETRGRDSPPTITIPVNINHAASGSFRESVDAQEEIRKVEKRATYVHKDGLNSTDHMVPDTESYDAVEIIRKVAVPPRLSEHTQRYEAANRTVQMAENFVNDPENEINRWFREFEHGPVSEAKSNRRVYAKGETNHNIQQESRTFCKEEFGLTSLGNTSFTDFSCKHPRELREKIPVKQPRICSETRSLSEHFSGMDAFESQIVESKMKTSSSHSSEAGKSGCDFKHAPPTYEDVIAGHILDISDSPKEVRKNFQKTWQESGRVFKGLGYATADASATEMRTTFQEESAFISEAAAPRQGNMYTLSKDSLSNGVPSGRQAEFS"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9#A4UGR9-2", 
            "isoform_ac": "A4UGR9-2", 
            "locus": {
                "end_pos": 167210839, 
                "strand": "-", 
                "start_pos": 167254123, 
                "chromosome": "2", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENST00000409273", 
                        "id": "ENST00000409273", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSP00000387255", 
                        "id": "ENSP00000387255", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "sp|A4UGR9-2|XIRP2_HUMAN Isoform 2 of Xin actin-binding repeat-containing protein 2  OS=Homo sapiens OX=9606 GN=XIRP2 PE=1 SV=2 CANONICAL=A4UGR9-1", 
                "length": 3327, 
                "sequence": "MARYQAAVSRGDCRSFSANMMEESEMCAVPGGLAKVKKQFEDEITSSRNTFAQYQYQHQNRSEQEAIHSSQVGTSRSSQEMARNEQEGSKVQKIDVHGTEMVSHLEKHTEEVNQASQFHQYVQETVIDTPEDEEIPKVSTKLLKEQFEKSAQEKILYSDKEMTTPAKQIKTESEYEETFKPSSVVSTSSTSCVSTSQRKETSTTRYSDHSVTSSTLAQINATSSGMTEEFPPPPPDVLQTSVDVTAFSQSPELPSPPRRLPVPKDVYSKQRNLYELNRLYKHIHPELRKNLEKDYISEVSEIVSSQMNSGSSVSADVQQARYVFENTNDSSQKDLNSEREYLEWDEILKGEVQSIRWIFENQPLDSINNGSPDEGDISRGIADQEIIAGGDVKYTTWMFETQPIDTLGAYSSDTVENAEKIPELARGDVCTARWMFETRPLDSMNKMHQSQEESAVTISKDITGGDVKTVRYMFETQHLDQLGQLHSVDEVHLLQLRSELKEIKGNVKRSIKCFETQPLYVIRDGSGQMLEIKTVHREDVEKGDVRTARWMFETQPLDTINKDITEIKVVRGISMEENVKGGVSKAKWLFETQPLEKIKESEEVIIEKEKIIGTDVSRKCWMFETQPLDILKEVPDADSLQREEIIGGDVQTTKHLFETLPIEALKDSPDIGKLQKITASEEEKGDVRHQKWIFETQPLEDIRKDKKEYTRTVKLEEVDRGDVKNYTHIFESNNLIKFDASHKIEVEGVTRGAVELNKSLFETTPLYAIQDPLGKYHQVKTVQQEEIVRGDVRSCRWLFETRPIDQFDESIHKFQIIRGISAQEIQTGNVKSAKWLFETQPLDSIKYFSDVEETESKTEQTRDIVKGDVKTCKWLFETQPMESLYEKVSLMTSSEEIHKGDVKTCTWLFETQPLDTIKDDSETAVKLQTVKQEEIQGGDVRTACFLFETENLDSIQGEEVKEIKPVEMDIQAGDVSSMRYKFENQSLDSISSSSEEVLKKIKTLKTEDIQKGNVLNCRWLFENQPIDKIKESQEGDECVKTVTDIQGGDVRKGCFIFETFSLDEIKEESDYISTKKTITEEVIQGDVKSYRMLFETQPLYAIQDREGSYHEVTTVKKEEVIHGDVRGTRWLFETKPLDSINKSETVYVIKSVTQEDIQKGDVSSVRYRFETQPLDQISEESHNIMPSIDHIQGGNVKTSRQFFESENFDKNNYIRTVSVNEIQKGNVKTSTWLFETHTMDELRGEGLEYENIKTVTQEDVQKGDVKQAVWLFENRTFDSIMEAHKGITKMTKEEIPPSDVKTTTWLFETTPLHEFNETRVEKIEIIGKSIKETLEDLYSQKVIQAPGIIIEADEIGDVRMAKYKLMNQASPEIQKEEIIRADLRNIMVNLLSKRDCTEREILISEEEKGNVNLTKTQLLNRSTEFHAEKEEIVKGDVQQAIKNLFSEERSVKKGILIQEDEKGDINMTIYCLLHENDGDTIEREEVIGGDVKRTIHNLLSSTSNNKISERAKIDASERGNVQFFTTCIEAGALDYLKQLHTESNETLTAKKQEGEKEIIGGDVEGTKLLLKKRQSLVERTVSETDIIPGDVHNTVKVFMTEPQSTFGKIPKEEIIKGDLTSTLNSLSQAVNQKTVTKTEEIIKGNMLATLKSLKESSHRWKESKQPDAIPGDIEKAIECLEKATNTKTEILKKELLKDDLETSLRSLKEAQRSFKEVHKEGVIKKDAKAVMAGSSGEQKTDIHQVAVQRNKNSLLQPKPGPFEPAAKWQGGADTLSQTMGKSCHGNLVEERTEVNLPKAPKGTVKIVIDREQNNDALEKSLRRLSNSHHKSNVLESGDKTGVWTDTTGEQHLRDEYMSRQLTSTVSVKNNLTTKESDRAVRELKKDDVFNSIQSAGKTVGKQQTYELRNDHQKMEGFHIKSPKKTKNIKILTDTQSSKPSPTQHPVSMPVGGTYDLSGDFQKQTLLKQETKYSNKDIKKKNINLQPMWQLLPVEQDTSNVTEMKVSEKSHNTFKATNKKRETDVHLKSQDFLMKTNTSTGLKMAMERSLNPINFNPENNVKESECPLPPPSPPPPPPSNASSEIEFPLPPPPPLMMFPEKNGFLPSLSTEKIKAEFESFPGLPLPPPPVDEKSERESSSMFLPPPPPPTPSQKPAHLLSSSAPEKHSGDFMQQYSQKEASNSQNSQAKIITGKTGVLPPPTLPKPKLPKHIKDNKNDFSPKVELATSLSDMECKITTSKDQKKVMVMTSSEHTETKQNVISKSLDERKQLSIDSANCLSHTVPGTSAPRKKQIAPLIKSHSFPESSGQQNPKPYMRKFKTPLMIAEEKYRQQKEEIEKQKQESSYYNIVKTQSQNQHITEVEKEMPLQKTNEEVSLSGIDSECTVVQPSPGSQSNARILGVCSDNQLSTTSPETVAAKRLHHVLAASEDKDKMKKEVLQSSRDIMQSKSACEIKQSHQECSTQQTQQKKYLEQLHLPQSKPISPNFKVKTIKLPTLDHTLNETDHSYESHKQQSEIDVQTFTKKQYLKTKKTEASTECSHKQSLAERHYQLPKKEKRVTVQLPTESIQKNQEDKLKMVPRKQREFSGSDRGKLPGSEEKNQGPSMIGRKEERLITERKHEHLKNKSAPKVVKQKVIDAHLDSQTQNFQQTQIQTAESKAEHKKLPQPYNSLQEEKCLEVKGIQEKQVFSNTKDSKQEITQNKSFFSSVKESQRDDGKGALNIVEFLRKREELQQILSRVKQFEAEPNKSGLKTFQTLLNTIPGWLISEDKREYAVHIAMENNLEKVKEEITHIKTQAEDMLVSYENIIQTAMMSSKTGKPGNKPTSLDETSSKVSNVHVSNNKNSEQKENKIAKEKTVQHQVAAHHEATVRSHVKTHQEIKLDDSNIPPPSLKTRPPSPTFITIESTARRTENPTKNELSQSPKKDSYVEPPPRRPMSQKSEIHRANTSPSPPRSRSEQLVRLKDTTAKLSKGAIPCPAATPVPIVEKRSEIIMSPATLRRQIKIETRGRDSPPTITIPVNINHAASGSFRESVDAQEEIRKVEKRATYVHKDGLNSTDHMVPDTESYDAVEIIRKVAVPPRLSEHTQRYEAANRTVQMAENFVNDPENEINRWFREFEHGPVSEAKSNRRVYAKGETNHNIQQESRTFCKEEFGLTSLGNTSFTDFSCKHPRELREKIPVKQPRICSETRSLSEHFSGMDAFESQIVESKMKTSSSHSSEAGKSGCDFKHAPPTYEDVIAGHILDISDSPKEVRKNFQKTWQESGRVFKGLGYATADASATEMRTTFQEESAFISEAAAPRQGNMYTLSKDSLSNGVPSGRQAEFS"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9#A4UGR9-3", 
            "isoform_ac": "A4UGR9-3", 
            "locus": {}, 
            "sequence": {
                "header": "sp|A4UGR9-3|XIRP2_HUMAN Isoform 3 of Xin actin-binding repeat-containing protein 2  OS=Homo sapiens OX=9606 GN=XIRP2 PE=1 SV=2 CANONICAL=A4UGR9-1", 
                "length": 3345, 
                "sequence": "MSPESGHSRIFEATAGPNKPESGFAEDSAARGEGVSDLHEVVSLKERMARYQAAVSRGDCRSFSANMMEESEMCAVPGGLAKVKKQFEDEITSSRNTFAQYQYQHQNRSEQEAIHSSQVGTSRSSQEMARNEQEGSKVQKIDVHGTEMVSHLEKHTEEVNQASQFHQYVQETVIDTPEDEEIPKVSTKLLKEQFEKSAQEKILYSDKEMTTPAKQIKTESEYEETFKPSSVVSTSSTSCVSTSQRKETSTTRYSDHSVTSSTLAQINATSSGMTEEFPPPPPDVLQTSVDVTAFSQSPELPSPPRRLPVPKDVYSKQRNLYELNRLYKHIHPELRKNLEKDYISEVSEIVSSQMNSGSSVSADVQQARYVFENTNDSSQKDLNSEREYLEWDEILKGEVQSIRWIFENQPLDSINNGSPDEGDISRGIADQEIIAGGDVKYTTWMFETQPIDTLGAYSSDTVENAEKIPELARGDVCTARWMFETRPLDSMNKMHQSQEESAVTISKDITGGDVKTVRYMFETQHLDQLGQLHSVDEVHLLQLRSELKEIKGNVKRSIKCFETQPLYVIRDGSGQMLEIKTVHREDVEKGDVRTARWMFETQPLDTINKDITEIKVVRGISMEENVKGGVSKAKWLFETQPLEKIKESEEVIIEKEKIIGTDVSRKCWMFETQPLDILKEVPDADSLQREEIIGGDVQTTKHLFETLPIEALKDSPDIGKLQKITASEEEKGDVRHQKWIFETQPLEDIRKDKKEYTRTVKLEEVDRGDVKNYTHIFESNNLIKFDASHKIEVEGVTRGAVELNKSLFETTPLYAIQDPLGKYHQVKTVQQEEIVRGDVRSCRWLFETRPIDQFDESIHKFQIIRGISAQEIQTGNVKSAKWLFETQPLDSIKYFSDVEETESKTEQTRDIVKGDVKTCKWLFETQPMESLYEKVSLMTSSEEIHKGDVKTCTWLFETQPLDTIKDDSETAVKLQTVKQEEIQGGDVRTACFLFETENLDSIQGEEVKEIKPVEMDIQAGDVSSMRYKFENQSLDSISSSSEEVLKKIKTLKTEDIQKGNVLNCRWLFENQPIDKIKESQEGDECVKTVTDIQGGDVRKGCFIFETFSLDEIKEESDYISTKKTITEEVIQGDVKSYRMLFETQPLYAIQDREGSYHEVTTVKKEEVIHGDVRGTRWLFETKPLDSINKSETVYVIKSVTQEDIQKGDVSSVRYRFETQPLDQISEESHNIMPSIDHIQGGNVKTSRQFFESENFDKNNYIRTVSVNEIQKGNVKTSTWLFETHTMDELRGEGLEYENIKTVTQEDVQKGDVKQAVWLFENRTFDSIMEAHKGITKMTKEEIPPSDVKTTTWLFETTPLHEFNETRVEKIEIIGKSIKETLEDLYSQKVIQAPGIIIEADEIGDVRMAKYKLMNQASPEIQKEEIIRADLRNIMVNLLSKRDCTEREILISEEEKGNVNLTKTQLLNRSTEFHAEKEEIVKGDVQQAIKNLFSEERSVKKGILIQEDEKGDINMTIYCLLHENDGDTIEREEVIGGDVKRTIHNLLSSTSNNKISERAKIDASERGNVQFFTTCIEAGALDYLKQLHTESNETLTAKKQEGEKEIIGGDVEGTKLLLKKRQSLVERTVSETDIIPGDVHNTVKVFMTEPQSTFGKIPKEEIIKGDLTSTLNSLSQAVNQKTVTKTEEIIKGNMLATLKSLKESSHRWKESKQPDAIPGDIEKAIECLEKATNTKTEILKKELLKDDLETSLRSLKEAQRSFKEVHKEGVIKKDAKAVMAGSSGEQKTDIHQVAVQRNKNSLLQPKPGPFEPAAKWQGGADTLSQTMGKSCHGNLVEERTEVNLPKAPKGTVKIVIDREQNNDALEKSLRRLSNSHHKSNVLESGDKTGVWTDTTGEQHLRDEYMSRQLTSTVSVKNNLTTKESDRAVRELKKDDVFNSIQSAGKTVGKQQTYELRNDHQKMEGFHIKSPKKTKNIKILTDTQSSKPSPTQHPVSMPVGGTYDLSGDFQKQTLLKQETKYSNKDIKKKNINLQPMWQLLPVEQDTSNVTEMKVSEKSHNTFKATNKKRETDVHLKSQDFLMKTNTSTGLKMAMERSLNPINFNPENNVKESECPLPPPSPPPPPPSNASSEIEFPLPPPPPLMMFPEKNGFLPSLSTEKIKAEFESFPGLPLPPPPVDEKSERESSSMFLPPPPPPTPSQKPAHLLSSSAPEKHSGDFMQQYSQKEASNSQNSQAKIITGKTGVLPPPTLPKPKLPKHIKDNKNDFSPKVELATSLSDMECKITTSKDQKKVMVMTSSEHTETKQNVISKSLDERKQLSIDSANCLSHTVPGTSAPRKKQIAPLIKSHSFPESSGQQNPKPYMRKFKTPLMIAEEKYRQQKEEIEKQKQESSYYNIVKTQSQNQHITEVEKEMPLQKTNEEVSLSGIDSECTVVQPSPGSQSNARILGVCSDNQLSTTSPETVAAKRLHHVLAASEDKDKMKKEVLQSSRDIMQSKSACEIKQSHQECSTQQTQQKKYLEQLHLPQSKPISPNFKVKTIKLPTLDHTLNETDHSYESHKQQSEIDVQTFTKKQYLKTKKTEASTECSHKQSLAERHYQLPKKEKRVTVQLPTESIQKNQEDKLKMVPRKQREFSGSDRGKLPGSEEKNQGPSMIGRKEERLITERKHEHLKNKSAPKVVKQKVIDAHLDSQTQNFQQTQIQTAESKAEHKKLPQPYNSLQEEKCLEVKGIQEKQVFSNTKDSKQEITQNKSFFSSVKESQRDDGKGALNIVEFLRKREELQQILSRVKQFEAEPNKSGLKTFQTLLNTIPGWLISEDKREYAVHIAMENNLEKVKEEITHIKTQAEDMLVSYENIIQTAMMSSKTGKPGNKPTSLDETSSKVSNVHVSNNKNSEQKENKIAKEKTVQHQVAAHHEATVRSHVKTHQEIKLDDSNIPPPSLKTRPPSPTFITIESTARRTENPTKNELSQSPKKDSYVEPPPRRPMSQKSEIHRANTSPSPPRSRSEQLVRLKDTTAKLSKGAIPCPAATPVPIVEKRSEIIMSPATLRRQIKIETRGRDSPPTITIPVNINHAASGSFRESVDAQEEIRKVEKRATYVHKDGLNSTDHMVPDTESYDAVEIIRKVAVPPRLSEHTQRYEAANRTVQMAENFVNDPENEINRWFREFEHGPVSEAKSNRRVYAKGETNHNIQQESRTFCKEEFGLTSLGNTSFTDFSCKHPRELREKIPVKQPRICSETRSLSEHFSGMDAFESQIVESKMKTSSSHSSEAGKSGCDFKHAPPTYEDVIAGHILDISDSPKEVRKNFQKTWQESGRVFKGLGYATADASATEMRTTFQEESAFISGK"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9#A4UGR9-4", 
            "isoform_ac": "A4UGR9-4", 
            "locus": {
                "end_pos": 166903483, 
                "strand": "-", 
                "start_pos": 167259360, 
                "chromosome": "2", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENST00000409043", 
                        "id": "ENST00000409043", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSP00000386454", 
                        "id": "ENSP00000386454", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "sp|A4UGR9-4|XIRP2_HUMAN Isoform 4 of Xin actin-binding repeat-containing protein 2  OS=Homo sapiens OX=9606 GN=XIRP2 PE=1 SV=2 CANONICAL=A4UGR9-1", 
                "length": 938, 
                "sequence": "MFPMQKGSLNLLRQKWESCDYQRSECHPRDSHCTIFQPQESKLLAPEGEVVSAPQSLDPTSLPYSTGEEMWSSKPEEKDSVDKSNNTREYGRPEVLKEDSLSSRRRIERFSIALDELRSVFEAPKSGNKPAEYGGKEVEIERSLCSPAFKSHPGSQLEDSVKDSDKKGKETSFDKMSPESGHSRIFEATAGPNKPESGFAEDSAARGEGVSDLHEVVSLKERMARYQAAVSRGDCRSFSANMMEESEMCAVPGGLAKVKKQFEDEITSSRNTFAQYQYQHQNRSEQEAIHSSQVGTSRSSQEMARNEQEGSKVQKIDVHGTEMVSHLEKHTEEVNQASQFHQYVQETVIDTPEDEEIPKVSTKLLKEQFEKSAQEKILYSDKEMTTPAKQIKKLLLQDKEICILCQKTVYPMECLVADKQNFHKSCFRCHHCNSKLSLGNYASLHGQIYCKPHFKQLFKSKGNYDEGFGHKQHKDRWNCKNQSRSVDFIPNEEPNMCKNIAENTLVPGDRNEHLDAGNSEGQRNDLRKLGERGKLKVIWPPSKEIPKKTLPFEEELKMSKPKWPPEMTTLLSPEFKSESLLEDVRTPENKGQRQDHFPFLQPYLQSTHVCQKEDVIGIKEMKMPEGRKDEKKEGRKNVQDRPSEAEDTKSNRKSAMDLNDNNNVIVQSAEKEKNEKTNQTNGAEVLQVTNTDDEMMPENHKENLNKNNNNNYVAVSYLNNCRQKTSILEFLDLLPLSSEANDTANEYEIEKLENTSRISELLGIFESEKTYSRNVLAMALKKQTDRAAAGSPVQPAPKPSLSRGLMVKGGSSIISPDTNLLNIKGSHSKSKNLHFFFSNTVKITAFSKKNENIFNCDLIDSVDQIKNMPCLDLREFGKDVKPWHVETTEAARNNENTGFDALSHECTAKPLFPRVEVQSEQLTVEEQIKRNRCYSDTE"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9#A4UGR9-5", 
            "isoform_ac": "A4UGR9-5", 
            "locus": {}, 
            "sequence": {
                "header": "sp|A4UGR9-5|XIRP2_HUMAN Isoform 5 of Xin actin-binding repeat-containing protein 2  OS=Homo sapiens OX=9606 GN=XIRP2 PE=1 SV=2 CANONICAL=A4UGR9-1", 
                "length": 763, 
                "sequence": "MSPESGHSRIFEATAGPNKPESGFAEDSAARGEGVSDLHEVVSLKERMARYQAAVSRGDCRSFSANMMEESEMCAVPGGLAKVKKQFEDEITSSRNTFAQYQYQHQNRSEQEAIHSSQVGTSRSSQEMARNEQEGSKVQKIDVHGTEMVSHLEKHTEEVNQASQFHQYVQETVIDTPEDEEIPKVSTKLLKEQFEKSAQEKILYSDKEMTTPAKQIKKLLLQDKEICILCQKTVYPMECLVADKQNFHKSCFRCHHCNSKLSLGNYASLHGQIYCKPHFKQLFKSKGNYDEGFGHKQHKDRWNCKNQSRSVDFIPNEEPNMCKNIAENTLVPGDRNEHLDAGNSEGQRNDLRKLGERGKLKVIWPPSKEIPKKTLPFEEELKMSKPKWPPEMTTLLSPEFKSESLLEDVRTPENKGQRQDHFPFLQPYLQSTHVCQKEDVIGIKEMKMPEGRKDEKKEGRKNVQDRPSEAEDTKSNRKSAMDLNDNNNVIVQSAEKEKNEKTNQTNGAEVLQVTNTDDEMMPENHKENLNKNNNNNYVAVSYLNNCRQKTSILEFLDLLPLSSEANDTANEYEIEKLENTSRISELLGIFESEKTYSRNVLAMALKKQTDRAAAGSPVQPAPKPSLSRGLMVKGGSSIISPDTNLLNIKGSHSKSKNLHFFFSNTVKITAFSKKNENIFNCDLIDSVDQIKNMPCLDLREFGKDVKPWHVETTEAARNNENTGFDALSHECTAKPLFPRVEVQSEQLTVEEQIKRNRCYSDTE"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9#A4UGR9-6", 
            "isoform_ac": "A4UGR9-6", 
            "locus": {
                "end_pos": 166903483, 
                "strand": "-", 
                "start_pos": 167259360, 
                "chromosome": "2", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENST00000409728", 
                        "id": "ENST00000409728", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSP00000386619", 
                        "id": "ENSP00000386619", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "sp|A4UGR9-6|XIRP2_HUMAN Isoform 6 of Xin actin-binding repeat-containing protein 2  OS=Homo sapiens OX=9606 GN=XIRP2 PE=1 SV=2 CANONICAL=A4UGR9-1", 
                "length": 971, 
                "sequence": "MFPMQKGSLNLLRQKWESCDYQRSECHPRDSHCTIFQPQESKLLAPEGEVVSAPQSLDPTSLPYSTGEEMWSSKPEEKDSVDKSNNTREYGRPEVLKEDSLSSRRRIERFSIALDELRSVFEAPKSGNKPAEYGGKEVEIERSLCSPAFKSHPGSQLEDSVKDSDKKGKETSFDKMSPESGHSRIFEAVFSTDQAQILRLHLHPKLTKTPKNSLKSSTYISTAGPNKPESGFAEDSAARGEGVSDLHEVVSLKERMARYQAAVSRGDCRSFSANMMEESEMCAVPGGLAKVKKQFEDEITSSRNTFAQYQYQHQNRSEQEAIHSSQVGTSRSSQEMARNEQEGSKVQKIDVHGTEMVSHLEKHTEEVNQASQFHQYVQETVIDTPEDEEIPKVSTKLLKEQFEKSAQEKILYSDKEMTTPAKQIKKLLLQDKEICILCQKTVYPMECLVADKQNFHKSCFRCHHCNSKLSLGNYASLHGQIYCKPHFKQLFKSKGNYDEGFGHKQHKDRWNCKNQSRSVDFIPNEEPNMCKNIAENTLVPGDRNEHLDAGNSEGQRNDLRKLGERGKLKVIWPPSKEIPKKTLPFEEELKMSKPKWPPEMTTLLSPEFKSESLLEDVRTPENKGQRQDHFPFLQPYLQSTHVCQKEDVIGIKEMKMPEGRKDEKKEGRKNVQDRPSEAEDTKSNRKSAMDLNDNNNVIVQSAEKEKNEKTNQTNGAEVLQVTNTDDEMMPENHKENLNKNNNNNYVAVSYLNNCRQKTSILEFLDLLPLSSEANDTANEYEIEKLENTSRISELLGIFESEKTYSRNVLAMALKKQTDRAAAGSPVQPAPKPSLSRGLMVKGGSSIISPDTNLLNIKGSHSKSKNLHFFFSNTVKITAFSKKNENIFNCDLIDSVDQIKNMPCLDLREFGKDVKPWHVETTEAARNNENTGFDALSHECTAKPLFPRVEVQSEQLTVEEQIKRNRCYSDTE"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9#A4UGR9-7", 
            "isoform_ac": "A4UGR9-7", 
            "locus": {
                "end_pos": 167210839, 
                "strand": "-", 
                "start_pos": 167259360, 
                "chromosome": "2", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENST00000409605", 
                        "id": "ENST00000409605", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSP00000386981", 
                        "id": "ENSP00000386981", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "sp|A4UGR9-7|XIRP2_HUMAN Isoform 7 of Xin actin-binding repeat-containing protein 2  OS=Homo sapiens OX=9606 GN=XIRP2 PE=1 SV=2 CANONICAL=A4UGR9-1", 
                "length": 716, 
                "sequence": "MARYQAAVSRGDCRSFSANMMEESEMCAVPGGLAKVKKQFEDEITSSRNTFAQYQYQHQNRSEQEAIHSSQVGTSRSSQEMARNEQEGSKVQKIDVHGTEMVSHLEKHTEEVNQASQFHQYVQETVIDTPEDEEIPKVSTKLLKEQFEKSAQEKILYSDKEMTTPAKQIKKLLLQDKEICILCQKTVYPMECLVADKQNFHKSCFRCHHCNSKLSLGNYASLHGQIYCKPHFKQLFKSKGNYDEGFGHKQHKDRWNCKNQSRSVDFIPNEEPNMCKNIAENTLVPGDRNEHLDAGNSEGQRNDLRKLGERGKLKVIWPPSKEIPKKTLPFEEELKMSKPKWPPEMTTLLSPEFKSESLLEDVRTPENKGQRQDHFPFLQPYLQSTHVCQKEDVIGIKEMKMPEGRKDEKKEGRKNVQDRPSEAEDTKSNRKSAMDLNDNNNVIVQSAEKEKNEKTNQTNGAEVLQVTNTDDEMMPENHKENLNKNNNNNYVAVSYLNNCRQKTSILEFLDLLPLSSEANDTANEYEIEKLENTSRISELLGIFESEKTYSRNVLAMALKKQTDRAAAGSPVQPAPKPSLSRGLMVKGGSSIISPDTNLLNIKGSHSKSKNLHFFFSNTVKITAFSKKNENIFNCDLIDSVDQIKNMPCLDLREFGKDVKPWHVETTEAARNNENTGFDALSHECTAKPLFPRVEVQSEQLTVEEQIKRNRCYSDTE"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9#A4UGR9-8", 
            "isoform_ac": "A4UGR9-8", 
            "locus": {
                "end_pos": 166903483, 
                "strand": "-", 
                "start_pos": 167254123, 
                "chromosome": "2", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENST00000409195", 
                        "id": "ENST00000409195", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSP00000386840", 
                        "id": "ENSP00000386840", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "sp|A4UGR9-8|XIRP2_HUMAN Isoform 8 of Xin actin-binding repeat-containing protein 2  OS=Homo sapiens OX=9606 GN=XIRP2 PE=1 SV=2 CANONICAL=A4UGR9-1", 
                "length": 3549, 
                "sequence": "MFPMQKGSLNLLRQKWESCDYQRSECHPRDSHCTIFQPQESKLLAPEGEVVSAPQSLDPTSLPYSTGEEMWSSKPEEKDSVDKSNNTREYGRPEVLKEDSLSSRRRIERFSIALDELRSVFEAPKSGNKPAEYGGKEVEIERSLCSPAFKSHPGSQLEDSVKDSDKKGKETSFDKMSPESGHSRIFEATAGPNKPESGFAEDSAARGEGVSDLHEVVSLKERMARYQAAVSRGDCRSFSANMMEESEMCAVPGGLAKVKKQFEDEITSSRNTFAQYQYQHQNRSEQEAIHSSQVGTSRSSQEMARNEQEGSKVQKIDVHGTEMVSHLEKHTEEVNQASQFHQYVQETVIDTPEDEEIPKVSTKLLKEQFEKSAQEKILYSDKEMTTPAKQIKTESEYEETFKPSSVVSTSSTSCVSTSQRKETSTTRYSDHSVTSSTLAQINATSSGMTEEFPPPPPDVLQTSVDVTAFSQSPELPSPPRRLPVPKDVYSKQRNLYELNRLYKHIHPELRKNLEKDYISEVSEIVSSQMNSGSSVSADVQQARYVFENTNDSSQKDLNSEREYLEWDEILKGEVQSIRWIFENQPLDSINNGSPDEGDISRGIADQEIIAGGDVKYTTWMFETQPIDTLGAYSSDTVENAEKIPELARGDVCTARWMFETRPLDSMNKMHQSQEESAVTISKDITGGDVKTVRYMFETQHLDQLGQLHSVDEVHLLQLRSELKEIKGNVKRSIKCFETQPLYVIRDGSGQMLEIKTVHREDVEKGDVRTARWMFETQPLDTINKDITEIKVVRGISMEENVKGGVSKAKWLFETQPLEKIKESEEVIIEKEKIIGTDVSRKCWMFETQPLDILKEVPDADSLQREEIIGGDVQTTKHLFETLPIEALKDSPDIGKLQKITASEEEKGDVRHQKWIFETQPLEDIRKDKKEYTRTVKLEEVDRGDVKNYTHIFESNNLIKFDASHKIEVEGVTRGAVELNKSLFETTPLYAIQDPLGKYHQVKTVQQEEIVRGDVRSCRWLFETRPIDQFDESIHKFQIIRGISAQEIQTGNVKSAKWLFETQPLDSIKYFSDVEETESKTEQTRDIVKGDVKTCKWLFETQPMESLYEKVSLMTSSEEIHKGDVKTCTWLFETQPLDTIKDDSETAVKLQTVKQEEIQGGDVRTACFLFETENLDSIQGEEVKEIKPVEMDIQAGDVSSMRYKFENQSLDSISSSSEEVLKKIKTLKTEDIQKGNVLNCRWLFENQPIDKIKESQEGDECVKTVTDIQGGDVRKGCFIFETFSLDEIKEESDYISTKKTITEEVIQGDVKSYRMLFETQPLYAIQDREGSYHEVTTVKKEEVIHGDVRGTRWLFETKPLDSINKSETVYVIKSVTQEDIQKGDVSSVRYRFETQPLDQISEESHNIMPSIDHIQGGNVKTSRQFFESENFDKNNYIRTVSVNEIQKGNVKTSTWLFETHTMDELRGEGLEYENIKTVTQEDVQKGDVKQAVWLFENRTFDSIMEAHKGITKMTKEEIPPSDVKTTTWLFETTPLHEFNETRVEKIEIIGKSIKETLEDLYSQKVIQAPGIIIEADEIGDVRMAKYKLMNQASPEIQKEEIIRADLRNIMVNLLSKRDCTEREILISEEEKGNVNLTKTQLLNRSTEFHAEKEEIVKGDVQQAIKNLFSEERSVKKGILIQEDEKGDINMTIYCLLHENDGDTIEREEVIGGDVKRTIHNLLSSTSNNKISERAKIDASERGNVQFFTTCIEAGALDYLKQLHTESNETLTAKKQEGEKEIIGGDVEGTKLLLKKRQSLVERTVSETDIIPGDVHNTVKVFMTEPQSTFGKIPKEEIIKGDLTSTLNSLSQAVNQKTVTKTEEIIKGNMLATLKSLKESSHRWKESKQPDAIPGDIEKAIECLEKATNTKTEILKKELLKDDLETSLRSLKEAQRSFKEVHKEGVIKKDAKAVMAGSSGEQKTDIHQVAVQRNKNSLLQPKPGPFEPAAKWQGGADTLSQTMGKSCHGNLVEERTEVNLPKAPKGTVKIVIDREQNNDALEKSLRRLSNSHHKSNVLESGDKTGVWTDTTGEQHLRDEYMSRQLTSTVSVKNNLTTKESDRAVRELKKDDVFNSIQSAGKTVGKQQTYELRNDHQKMEGFHIKSPKKTKNIKILTDTQSSKPSPTQHPVSMPVGGTYDLSGDFQKQTLLKQETKYSNKDIKKKNINLQPMWQLLPVEQDTSNVTEMKVSEKSHNTFKATNKKRETDVHLKSQDFLMKTNTSTGLKMAMERSLNPINFNPENNVKESECPLPPPSPPPPPPSNASSEIEFPLPPPPPLMMFPEKNGFLPSLSTEKIKAEFESFPGLPLPPPPVDEKSERESSSMFLPPPPPPTPSQKPAHLLSSSAPEKHSGDFMQQYSQKEASNSQNSQAKIITGKTGVLPPPTLPKPKLPKHIKDNKNDFSPKVELATSLSDMECKITTSKDQKKVMVMTSSEHTETKQNVISKSLDERKQLSIDSANCLSHTVPGTSAPRKKQIAPLIKSHSFPESSGQQNPKPYMRKFKTPLMIAEEKYRQQKEEIEKQKQESSYYNIVKTQSQNQHITEVEKEMPLQKTNEEVSLSGIDSECTVVQPSPGSQSNARILGVCSDNQLSTTSPETVAAKRLHHVLAASEDKDKMKKEVLQSSRDIMQSKSACEIKQSHQECSTQQTQQKKYLEQLHLPQSKPISPNFKVKTIKLPTLDHTLNETDHSYESHKQQSEIDVQTFTKKQYLKTKKTEASTECSHKQSLAERHYQLPKKEKRVTVQLPTESIQKNQEDKLKMVPRKQREFSGSDRGKLPGSEEKNQGPSMIGRKEERLITERKHEHLKNKSAPKVVKQKVIDAHLDSQTQNFQQTQIQTAESKAEHKKLPQPYNSLQEEKCLEVKGIQEKQVFSNTKDSKQEITQNKSFFSSVKESQRDDGKGALNIVEFLRKREELQQILSRVKQFEAEPNKSGLKTFQTLLNTIPGWLISEDKREYAVHIAMENNLEKVKEEITHIKTQAEDMLVSYENIIQTAMMSSKTGKPGNKPTSLDETSSKVSNVHVSNNKNSEQKENKIAKEKTVQHQVAAHHEATVRSHVKTHQEIKLDDSNIPPPSLKTRPPSPTFITIESTARRTENPTKNELSQSPKKDSYVEPPPRRPMSQKSEIHRANTSPSPPRSRSEQLVRLKDTTAKLSKGAIPCPAATPVPIVEKRSEIIMSPATLRRQIKIETRGRDSPPTITIPVNINHAASGSFRESVDAQEEIRKVEKRATYVHKDGLNSTDHMVPDTESYDAVEIIRKVAVPPRLSEHTQRYEAANRTVQMAENFVNDPENEINRWFREFEHGPVSEAKSNRRVYAKGETNHNIQQESRTFCKEEFGLTSLGNTSFTDFSCKHPRELREKIPVKQPRICSETRSLSEHFSGMDAFESQIVESKMKTSSSHSSEAGKSGCDFKHAPPTYEDVIAGHILDISDSPKEVRKNFQKTWQESGRVFKGLGYATADASATEMRTTFQEESAFISEAAAPRQGNMYTLSKDSLSNGVPSGRQAEFS"
            }
        }
    ], 
    "pathway": [
        {
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+hsa:129446", 
            "resource": "KEGG Pathway", 
            "id": "hsa:129446", 
            "name": ""
        }
    ], 
    "reaction_participants": [], 
    "function": [
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
            "annotation": "A genome-wide association study reveals 2 new susceptibility loci for atopic dermatitis, XIRP2 and DMRTA1.", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ]
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
            "annotation": "Genetic information from this patient implies that genes involved in development and maintenance of extraocular muscles can cause congenital ocular motility disorders as well.", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ]
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
            "annotation": "Observational study and genome-wide association study of gene-disease association. (HuGE Navigator)", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ]
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
            "annotation": "Observational study of gene-disease association. (HuGE Navigator)", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ]
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A0A5F9ZH43#function", 
            "annotation": "Protects actin filaments from depolymerization.", 
            "evidence": [
                {
                    "url": "https://www.uniprot.org/uniprot/A0A5F9ZH43#function", 
                    "id": "A0A5F9ZH43", 
                    "database": "UniProtKB"
                }
            ]
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A4UGR9#function", 
            "annotation": "Protects actin filaments from depolymerization.", 
            "evidence": [
                {
                    "url": "https://www.uniprot.org/uniprot/A4UGR9#function", 
                    "id": "A4UGR9", 
                    "database": "UniProtKB"
                }
            ]
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
            "annotation": "Report pathogenic XIRP1/2 rare variants in arrhythmogenic disorders such as sudden unexplained nocturnal death syndrome and Brugada syndrome. Publication Status: Online-Only", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ]
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
            "annotation": "Xin and XIRP2 define a novel actin-binding motif", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
                    "id": "NP_001073278.1", 
                    "database": "RefSeq"
                }
            ]
        }
    ], 
    "orthologs": [
        {
            "uniprot_canonical_ac": "Q4U4S6-1", 
            "protein_name": "Xin actin-binding repeat-containing protein 2", 
            "sequence": {
                "length": 3784, 
                "sequence": "MARYQAAVSRGDTRSFSANVMEESDVCTVPGGLAKMKRQFEKDKMTSTCNAFSEYQYRHESRAEQEAIHSSQEIIRRNEQEVSKGHGTDVFKAEMMSHLEKHTEETKQASQFHQYVQETVIDSPEEEELPKVSTKILKEQFEKSAQENFLRSDKETSPPAKCMKIENDIEETLKPSSAVGTSSSYTSTRQRKETSTSSYSNHSLTSTTLAQDNGTPSGKMEEFPPPPPDVCQTPMDVTAFSQSPEFPSPPRRLPMPKDLYSKQRNLYELNRLYRHIHPELRKNLEKDYISEVSEIVSSQINSGNALSADVQKARYVFENTNDSSQKDLNSERENLEWDEILKGEVQSIRWIFENQPLDSINHGSTDEGYTSKGIADQELIAGSDVKYTTWMFETQPIDALGIPSAGTEGNTEKIPELARGDVYTARWMFETRPLDSMNKMHECQEETASTLTKDITGGDVKTVRYMFETQQLDQLGQLHSVDELNLLQLRSELKEIKGNVKRSIKCFETQPLYVIRDGSGQMLEIKTVQREDIEKGDVRTARWMFETQPLDTINKDITEIKVVRGISMEENVKGGVSRAKWLFETQPLEKIKEESGEAVLKTEAVIGTDVSKKCWMFETQPLDILKDSPDTDSVSPEERIGGDVKTTKHLFETLPIEALKDSPDIGKLQKITASEEEKGDVKHQKWVFETQRLEDIREDKKEYTRTVRLEAVDRGHVKNYTHIFESNNLIKVDASHQIEVEGVTRGTVELNKSLFETTPLYAIQDHLGKYHQVKTVQQEEIVRGDVRSCRWLFETRPIDQFDESLHKFQIIRGISAQEIQAGNVKSARWLFETQPLDSIKYFSNVEETDSKTEQSTDIVKGDVKTCKWLFETQPMESLYEKASLMTNSEDIHKGDVRTCMWLFETQPLDAIKDDSEATVKLQTVKQEEIQGGDVQTACFLFETENLDNIQGDEGKENKPLEMDIQSGDVSGMKFKFENQSLDSINCSSENVLSKIKTLKAEDIQKGNVLKCRWLFENQPIDMIKESQECDGLVKTVTDVQGGDVRKGCFIFETFSLDEIKDESDGISMRETNLGEIIKGDVKSYKMLFETQPLYAIQDHEGFYHEVTTVKKEETIHGDVRGTRWLFETKPLDSIHESEDVYVIKSVTQEDIQKGDVSSVRYRFETQPLDMISDKSHNIVPTVDYIQGGNVQMNKQLFESEGGNKKNYVRTVSVNEIQKGNVKTSTWLFETHRIDELGEESRYENIKTVTQEDVQKGDVKQAVWLFENQTLDSINELDENDTKMTKEEIPPSDVKTTTWLFETTPIHEFNKTRVEKEEIIGKSIKETLEDLYSQRVVEAPGIIIEADEVGDVRMAKYKLMNQTTPEIQKEEVIRADLGNIMMNLLSQRDCTKKEIFVSEEEKGNVNFTKTQLLNRSMEFHAEKEEIVRGDVKQAIQKLFSEERRAKKGILIQEDEKGDINMTIYCLLHENAGDKTEREDILGGDVRRTIHNLLSSASNGKISERTKIDASERGNVQFFTTCIETGALDYLKQLQTGSNESTLTASKQEGEEEIIGGDVEGTKFLLKKRQSSFERTVSETDIIPGDVRHTVKVFMTEPQSSSYKTVKDEIIKGDLKSTLNSLNQAMNQKTVAKAEEIVKDDRLAILKSLKESGDRQKEPKQSGGMSRDIGQAIECLERATNTRTEILKKELILDDLKTSLRSLKEEQCGFKEVDKQGIVKDVLPGMLGFSERPKIGIHPAAVQRDKKSLLQPVPGPFEPAIKQQAGPGTLDETTQKPCLRSLIEERTEANLPKAPKGTVKIVIDREQNNDALEKSLRKMSNSEHRAMKNVLDMSDRMGIWTESKEYLCSDDHMSKHLSATMSIKESLKSKESENMREAKDDVISSTQSVDKTFRKQQTQTCELGNDQKSRFQDSYGKNQKNIQNIEITRDFQKQALLSQEKQYSNKEMKKNEASLQPLPVGKEVHSVPGVTVSGKNHKRIQATDKRQKTDVCLESQDFLMKTNTSKELKMAMERSFNPINLHPECGIKENEDSLPPPSPPPLPPSNASSEIEFPLPPPPPLMLLPGKNESPPSSPTEKTRTEFESLSTLPLPPPPVDEKAEQECLSTTLPPPPPPTPCQPGHLLPSSVLGHHREAFLQQFSQKEALGVHLPHSQAKILTGKSPPPTLPKPKLPKRIKDKMNQYSSSGELERSLSDVEIKATLSKDQKRSMVTMSSEHRETKQDVFGKGLVGRKQLPVDSANSLSQTVPEIPAPKEKQTAPLVKSHSFPSGSEQQSPKPYMRKFKTPLMIAEEKYRQQREELEKQRQESSSHNVIKTETQHQSLSEKEEEIELQKATEAISTPRKESDFPRARPNLDSESRAVIAGECSESQLATASTLTVATERLQHVLAASEDELTLRQEGIQNSSDASQSKLACETSQSHKECKAQQTFEQHVKRLPFPQTKPSSPSFKVKTIKLSTLDHTGTETDLSSKHHTKQSEVDIQTSTEQTDKEIKKTQASIQCDDKPSVPEKYFQLPKTEKRVTIQMPKEYAEKSHKSKLQTVPKKQGIFGEFDRGNVLGREGKNQDSSVSCSKEDRLIDERKQEHLQNQRVPRSVQQKVINERLDSQMQNFQQTEIQTSRSTIECEEFSQSYNATQEKTCLKDKGKQQGQVTSNTEESKQELRQNQSAFSSVKDSQHDDGKCTINILEFLRKREELQQILSRVKQFEAESSKSGLKTFQILLNIVPVWLISEEKREYGVRVAMENNFEKVKEEITHIKTQAEEMLLQCEHVIQTAMMASQTGKQRDKPTNLNEMPLNVSNVNLSSSKCTEQKESKTVEEKLTHRQVTTHPEAATRNPVKPYQEAKGEDGKMAPPSLKTRPPSPTFITIESTARRAETSTKSELSQSPKNNRCIEPPPRRPVEHASGLPRSRTPPSPPRSRSEQLVRLKDTTARLAKGTIPCSPGTPVPIVEKRSEVVMSPATLRRQIKIESRGGDSPPTITIPVSVNHVVSGSFRESVDAQEAVKKTEKTETYVHKDKMNSVNRAMPETESYDAVEIIRKVEGPHLSEHTERFEATNQTVQRAERFLNGHENEINRWFREFENDPVFRAKTERGAYANGEINHNMKQESHTFCKEEFGLASSETANFTGFSYRHPKVPAMQPRVHSEARSLNEHFSSVDAFDSQIVGSKVATSSSRSTEAGRSGFDFKHAPPTYEDVISGHILDVADSPTNLRRNFQKTWQESERVFQRVGYETSDAHATEMSRAFQEESAFLSDKEICIICQKTVYPMECLIADKQNFHKSCFRCHHCSSKLSLGNYASLHGRIYCKPHFKQLFKSKGNYDEGFGHKQHKDRWNCKNQSSLVDFIPSGEPDAHENPTADTLLLGDLTTHPDACNSKRQDNDLRKWGDRGKLKIVWPPCQEMPKKNSPPEEEFKVNKAKWPPEVTIPVPSDFKRESLTEHVKTLESQGQEQDSVPDLQPCKHVCQKEDITGIKEIKGYEERKDEKEAKDTLKDAEGLRSKRKSGMEFNDHNAHAQSDGKEKNALVNEADSADVLQVANTDDEGGPENHRENFNNNNNNSVAVSSLNNGRQKISISERPRLLQAVSEANYYTSEYQIKNFNNASKISELLGIFESQKLSSKKVLALALERTADRGTAGSPLQLVLEPGLQQGFSVKGENLAASPDVSPLHIKGNHENNKNVHLFFSNTVKITSFSKKHNILGCDLMDSVDQLKNMSCLYLRELGKNVKCWHGETAGAARHGGKMCFDAQSQGSAAKPVFPSMQCQAQHLTVEEQIKRDRCYSDSEAD"
            }, 
            "evidence": [
                {
                    "url": "http://www.informatics.jax.org/homology/19388", 
                    "id": "19388", 
                    "database": "MGI"
                }
            ], 
            "common_name": "Mouse", 
            "organism": "Mus musculus", 
            "gene_name": "Xirp2", 
            "tax_id": 10090
        }, 
        {
            "uniprot_canonical_ac": "Q71LX6-1", 
            "protein_name": "Xin actin-binding repeat-containing protein 2", 
            "sequence": {
                "length": 3302, 
                "sequence": "MARYQAAVSRGDTRSFSANVMEESDLCTVPGGLAKMKRQFEKDEMTSTCNAFSEYQYQHESRSEQEAIHNRQEIRRNEEEVSKGHRTDVFKAEMMSHLEKHTEETNQASQFRQYVQETVIDTPEDEEIPKVSTKILKEQFEKTAQENFLYSDKETTTPAKCIKIENDSEETLKPSSAMGTSSYTSARQSKETSTSSYSNHSLTSTILAQEKGTPSGKMEEFPPPPPDVFQTPMDVTAFSQSPEFPSPPRRLPMPRDVYSKQRNLYELNRLYRHIHPELRKNLEKDYISEVSEIVSSHINSGNSISAGVQQARYVFENTNDSSQKDLSSERENLEWDEILKGEVQSIRWIFENQPLDSINQGFTDEAYTSKGIADQELIAGGDVKYTTWMFETQPIDALGVPSAGTEENTEKIPELAKGDVCTARWMFETRPLDSMNKMHEWEDETASTFIKDITGGDVKTVRYMFETQQLDQLGQLHSVDEMNLLQLRSELKEIKGNVKRSIKCFETQPLYVIRDGSGQMLEIKTVQREDIEKGDVRTARWMFETQPLDTIKQDITEIKVVRGISMEENVKGEVGRARWLFETQPLEKIKEESGEAVLKTEAVVGIDVSKKCWMFETQPLDTLKQSPDTESVSPEERIGGDVKTTKHLLETLPIEALKDSPDVGKLQKITASEEEKGDVKHQKWVFETQRLEDIREDKKEYTQTVKLEAVDRGHVKNYTHIFESNNLIKVDASHQIEVEGVTRGTVELNKSLFETTPLYAIQDHLGKYHQVKTVQQEEIVRGDVRSCRWLFETRPIDQFDESLHKFQIIRGISAQEIQAGNVKSARWLFETQPLDSIKYFSNVEETDSKTEQSTDIVKGDVKTCKWLFETQPMESLYEKASLMTNSEDIHKGDVRTCMWLFETQPLDAIKNDSEATVKLQTVKQEEIQGGDVRTACLLFETENLDNIQGGEGKETKPVEMDIESGDVSGMKYKFENQSLDSISCSSENVLNKIKTLKIEDIQKGNVLNCRWLFENQPIDMIKENQEGDGLVKTVTDIQGGDVRKGCFIFETFSLDEIKDESDVISTRQTNTEEVIKGDVKSYKMLFETQPLYAIQDQEGFYHEVTTVKKEETIHGDVRGTRWLFETKPLDSINASEDVYIIKSVTQEDIQKGDVSSVRYRFETQPLDMISDKSHNIMPTIDHIQGGNVQMNKQLFESEGGDKKNYVRTVSINEIQKGNVKTSTWLFETHSIDELGEVSTYENIKTVTQEDVQKGDVKQAVWLFENQTLDSIKELDESDTKITKEEIPPSDVKTTTWLFETTPIHEFNETRIEKEEIIGKSIKETLEDLYSQRVVEAPGIIIEADEVGDVRMAKYKLMNQRTPEIQKEEVIRADLGNIMMNLLSQRDCTKKEIFISEEEKGNVNFTKTQLLNRSMEFHAEKEEIVRGDVKQAIQKLFSEERCAKRGILIQEDEKGDVNMTIYCLLHENAGDKTKREDILGGDVRRTIHNLLSSASNDKISERTKIDASERGNVQFFTTCIETGALDYLKQLQTGSNETLTARKQEGEEEIIGGDVEGTKFLLKKRQSSIERTVSETDIIPGDVRNTVKVFMTEPQSASFKTAKEEIVKGDLKSTLNSLNQAMNQKVVAKTEDIMKDDKAAILKSLKESGGRQKEHKQSASISSDIGQAIECLEKATNTRTEILKKELILDDLKTSLRSLKEEQYSFKEVGKQGMVKDVLGFSERQELGIHPAAVQREKKSLLQPVPGPCEPAIRQQAGPGPLDEATQKSCHRSLTEERTEANLPKAPKGTVKIVIDREQNNDALEKSLRKMSNSEHRAMKNVLDMGDRRGVWTESKECLCSDDHMSKYVSASMSRKKSLKTKESENVRESKDDVSSTQSVDKTFRKQQTQNCELGKDHQKSQFQDSYAKNQKNTQNISMSAETQSYRPDPTQHPVSNPAGETLEMTRDFQKQALIRQEKQNSNKDMRKNDMGLQPLPVGKDAHSAPGVTVSGKNHKRTQAPDKKQRIDVCLESQDFLMKTNTSKELKMAMERSFNPVNLYPDCGVKENEDALPPPSPPPPPPSNASSEIEFPLPPPPPIMLLPEKNEFPPSSPTEKSRAELESLPTLPLPPPPGDEKSDQECLPTSLPPPPPTAPSQPAHLLSSSVLEHHSEAFLQQYSRKETLDSHQLHSQAKILTGKSPPPTLPKPKLPERIKAKMSQDSPSGELERSLSDVEIKTTLSKDQKSSLVAESREHTEAKQEVFRKSLGRKQLSISSANSLSQTVPEIPAPKEKQTAPLVKSHSFPSGSEQQSPKPYMRKFKTPLMIAEEKYRQQREELEKQRRESSCHSIIKTETQHRSLSEKEKETELQKAAEAMSTPRKDSDFTRAQPNLEPKSKAVIASECSESQLSTASALTVATERLQHVLAASDDKLTLRREGTQNSSDTLQSKTACEINQSHKECRTEQTFEQHVEKLPFPQTKPISPSFKVKTIRLPALDHTLTETDLSSERRVKQSEIDVQTSTKEMNKEIKKTEVSTQCDNKQSVAEKYFQLPKTEKRVTVQMPKDYAAKSHQSKLQTVPKKHGGLGEFDRGNVLGREGKNQDSSMSSTKESRVIVERKQEHLQDQSVPRLVQQKIIGESLDSRVQNFQQTQTQTSRIEHKELSQPYSEKKCLRDKDKQQKQVSSNTDDSKQEITQKQSSFSSVRESQQDGEKCAINILEFLRKREELQQILSRVKQFEADSNKSGLKTFQTLLNIAPVWLISEEKREYGVRVAMENNLEKVKEEIIHIKTQAEEMLVHCEHVIRTAMMASQTGKQKDKPTNLNEMPLKVSNVNLSSHKGTEQKESKIVEEKLASRQVATHSEAATHNPAKTYQEAKGDDSKMAPPSLKTRPPSPTFITIESTARRAETSTKSELSQSPKNNSCVEPLPRRPMEHTSRLPRTSTSPSPPRSRSEQLVRLKDTTARLAKGTIPCSPGTPVPVVEKRSEVVMSPATLRRQIKIESRGGDSPPTITIPVSVNHHVVSGSFRESVDAQEAVKKTEKTETYVHKDKKNSVSSAMPETESYDAVEIIRKVEGPHLSEHRERFEATNQTVQMAEHFLNGHENEVNRWFREFENGPVFGAKTERRAYANGEINHNMKQESHTFCKEEFGLESSETANFTGFSYRHPREHRAKAPATQPRVHSEARALNEHFLSVDAFDSQIVESQVATSSSRSSEAGRSGFDFKHAPPTYEDVIAGHILDIADSPTNLRRNFQKTWQESERVFKSVGYETSDAHATEMSRAFQEELAFLSETVGPRQGNLHNLSKDGLSNGVPRSRPAEFS"
            }, 
            "evidence": [
                {
                    "url": "http://www.informatics.jax.org/homology/19388", 
                    "id": "19388", 
                    "database": "MGI"
                }
            ], 
            "common_name": "Rat", 
            "organism": "Rattus norvegicus", 
            "gene_name": "Xirp2", 
            "tax_id": 10116
        }
    ], 
    "interactions": [], 
    "synthesized_glycans": [], 
    "snv": [
        {
            "sequence_org": "S", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167245030G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs369227139", 
                    "id": "rs369227139", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs369227139", 
                    "id": "rs369227139", 
                    "database": "ExAC"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs369227139#frequency_tab", 
                    "id": "rs369227139", 
                    "database": "TOPMed"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain", 
                "o-glyco-site-loss"
            ], 
            "sequence_mut": "N", 
            "start_pos": 1038, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1038, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (SSS->NSS)."
        }, 
        {
            "sequence_org": "L", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "C", 
            "chr_pos": "167245243T>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs201086393", 
                    "id": "rs201086393", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs201086393", 
                    "id": "rs201086393", 
                    "database": "1000Genomes"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs201086393", 
                    "id": "rs201086393", 
                    "database": "ExAC"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs201086393#frequency_tab", 
                    "id": "rs201086393", 
                    "database": "TOPMed"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs201086393", 
                    "id": "rs201086393", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "S", 
            "start_pos": 1062, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1062, 
            "minor_allelic_frequency": "0.0002", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NVL->NVS)."
        }, 
        {
            "sequence_org": "R", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "C", 
            "chr_pos": "167245111G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200182549", 
                    "id": "rs200182549", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200182549", 
                    "id": "rs200182549", 
                    "database": "ExAC"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs200182549#frequency_tab", 
                    "id": "rs200182549", 
                    "database": "TOPMed"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs200182549", 
                    "id": "rs200182549", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "T", 
            "start_pos": 1065, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1065, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NCR->NCT)."
        }, 
        {
            "sequence_org": "K", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "C", 
            "chr_pos": "167245648A>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769431929", 
                    "id": "rs769431929", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769431929", 
                    "id": "rs769431929", 
                    "database": "ExAC"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs769431929", 
                    "id": "rs769431929", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "T", 
            "start_pos": 1244, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1244, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NVK->NVT)."
        }, 
        {
            "sequence_org": "K", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "C", 
            "chr_pos": "167245741A>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769577256", 
                    "id": "rs769577256", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769577256", 
                    "id": "rs769577256", 
                    "database": "ExAC"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs769577256#frequency_tab", 
                    "id": "rs769577256", 
                    "database": "TOPMed"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs769577256", 
                    "id": "rs769577256", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "T", 
            "start_pos": 1275, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1275, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NVK->NVT)."
        }, 
        {
            "sequence_org": "K", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "T", 
            "chr_pos": "167245925A>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs373164678", 
                    "id": "rs373164678", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs373164678", 
                    "id": "rs373164678", 
                    "database": "ExAC"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs373164678#frequency_tab", 
                    "id": "rs373164678", 
                    "database": "TOPMed"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs373164678", 
                    "id": "rs373164678", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain", 
                "o-glyco-site-loss"
            ], 
            "sequence_mut": "N", 
            "start_pos": 1336, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1336, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (KMT->NMT)."
        }, 
        {
            "sequence_org": "M", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "C", 
            "chr_pos": "167246218T>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs371974788", 
                    "id": "rs371974788", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs371974788", 
                    "id": "rs371974788", 
                    "database": "ExAC"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs371974788#frequency_tab", 
                    "id": "rs371974788", 
                    "database": "TOPMed"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs371974788", 
                    "id": "rs371974788", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "T", 
            "start_pos": 1434, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1434, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NIM->NIT)."
        }, 
        {
            "sequence_org": "D", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167246241G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751610409", 
                    "id": "rs751610409", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751610409", 
                    "id": "rs751610409", 
                    "database": "ExAC"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751610409", 
                    "id": "rs751610409", 
                    "database": "NCI-TCGA"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs751610409", 
                    "id": "rs751610409", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "N", 
            "start_pos": 1442, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1442, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (DCT->NCT)."
        }, 
        {
            "sequence_org": "G", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167246490G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1344729505", 
                    "id": "rs1344729505", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs1344729505", 
                    "id": "rs1344729505", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "S", 
            "start_pos": 1525, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1525, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NDG->NDS)."
        }, 
        {
            "sequence_org": "K", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "T", 
            "chr_pos": "167241862G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1240472781", 
                    "id": "rs1240472781", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs1240472781", 
                    "id": "rs1240472781", 
                    "database": "gnomAD"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs749100912", 
                    "id": "rs749100912", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs749100912", 
                    "id": "rs749100912", 
                    "database": "ExAC"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs749100912", 
                    "id": "rs749100912", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain", 
                "o-glyco-site-loss"
            ], 
            "sequence_mut": "N", 
            "start_pos": 154, 
            "keywords": [
                "ebi", 
                "somatic", 
                "germline"
            ], 
            "end_pos": 154, 
            "minor_allelic_frequency": "", 
            "annotation": "Somatic mutation passed 1 out of 1 filters: n-glyco-sequon-gain (KHT->NHT)."
        }, 
        {
            "sequence_org": "K", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "C", 
            "chr_pos": "167246575A>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1216369852", 
                    "id": "rs1216369852", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs1216369852", 
                    "id": "rs1216369852", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "T", 
            "start_pos": 1553, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1553, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NNK->NNT)."
        }, 
        {
            "sequence_org": "D", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167246598G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751843822", 
                    "id": "rs751843822", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751843822", 
                    "id": "rs751843822", 
                    "database": "ExAC"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs751843822", 
                    "id": "rs751843822", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "N", 
            "start_pos": 1561, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1561, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (DAS->NAS)."
        }, 
        {
            "sequence_org": "S", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167247385G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774499825", 
                    "id": "rs774499825", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774499825", 
                    "id": "rs774499825", 
                    "database": "ExAC"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs774499825#frequency_tab", 
                    "id": "rs774499825", 
                    "database": "TOPMed"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs774499825", 
                    "id": "rs774499825", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain", 
                "o-glyco-site-loss"
            ], 
            "sequence_mut": "N", 
            "start_pos": 1823, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1823, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (SQT->NQT)."
        }, 
        {
            "sequence_org": "P", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "T", 
            "chr_pos": "167247447C>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs868517861", 
                    "id": "rs868517861", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs868517861#frequency_tab", 
                    "id": "rs868517861", 
                    "database": "TOPMed"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "S", 
            "start_pos": 1844, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1844, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NLP->NLS)."
        }, 
        {
            "sequence_org": "I", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "C", 
            "chr_pos": "167247733T>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs113521008", 
                    "id": "rs113521008", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ensembl.org/id/rs113521008", 
                    "id": "rs113521008", 
                    "database": "ENSEMBL"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "T", 
            "start_pos": 1939, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 1939, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NSI->NST)."
        }, 
        {
            "sequence_org": "D", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167247921G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs113038974", 
                    "id": "rs113038974", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs113038974", 
                    "id": "rs113038974", 
                    "database": "ExAC"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs113038974", 
                    "id": "rs113038974", 
                    "database": "NCI-TCGA"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs113038974#frequency_tab", 
                    "id": "rs113038974", 
                    "database": "TOPMed"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs113038974", 
                    "id": "rs113038974", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "N", 
            "start_pos": 2002, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 2002, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (DLS->NLS)."
        }, 
        {
            "sequence_org": "N", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "C", 
            "chr_pos": "167248006A>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs73029762", 
                    "id": "rs73029762", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs73029762", 
                    "id": "rs73029762", 
                    "database": "1000Genomes"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs73029762", 
                    "id": "rs73029762", 
                    "database": "ExAC"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs73029762#frequency_tab", 
                    "id": "rs73029762", 
                    "database": "TOPMed"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs73029762", 
                    "id": "rs73029762", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "T", 
            "start_pos": 2030, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 2030, 
            "minor_allelic_frequency": "0.009185", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NIN->NIT)."
        }, 
        {
            "sequence_org": "N", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "G", 
            "chr_pos": "167248222A>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs746369776", 
                    "id": "rs746369776", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs746369776", 
                    "id": "rs746369776", 
                    "database": "ExAC"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs746369776#frequency_tab", 
                    "id": "rs746369776", 
                    "database": "TOPMed"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs746369776", 
                    "id": "rs746369776", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "S", 
            "start_pos": 2102, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 2102, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NFN->NFS)."
        }, 
        {
            "sequence_org": "D", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167248707G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs563915541", 
                    "id": "rs563915541", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs563915541", 
                    "id": "rs563915541", 
                    "database": "1000Genomes"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs563915541", 
                    "id": "rs563915541", 
                    "database": "ExAC"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs563915541", 
                    "id": "rs563915541", 
                    "database": "gnomAD"
                }
            ], 
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                "n-glyco-sequon-gain"
            ], 
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            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 2264, 
            "minor_allelic_frequency": "0.0002", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (DFS->NFS)."
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            "ref_nt": "A", 
            "chr_pos": "167249194T>", 
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                    "id": "rs377767168", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs377767168#frequency_tab", 
                    "id": "rs377767168", 
                    "database": "TOPMed"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs377767168", 
                    "id": "rs377767168", 
                    "database": "gnomAD"
                }
            ], 
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                "n-glyco-sequon-gain"
            ], 
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                "ebi", 
                "germline"
            ], 
            "end_pos": 2426, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (IDS->NDS)."
        }, 
        {
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            "alt_nt": "null", 
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            "chr_pos": "167242680G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs986502825", 
                    "id": "rs986502825", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ensembl.org/id/rs986502825", 
                    "id": "rs986502825", 
                    "database": "ENSEMBL"
                }
            ], 
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                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "N", 
            "start_pos": 255, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 255, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (DHS->NHS)."
        }, 
        {
            "sequence_org": "T", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167249617C>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1449979016", 
                    "id": "rs1449979016", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs1449979016", 
                    "id": "rs1449979016", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain", 
                "o-glyco-site-loss"
            ], 
            "sequence_mut": "N", 
            "start_pos": 2567, 
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                "ebi", 
                "germline"
            ], 
            "end_pos": 2567, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (TFT->NFT)."
        }, 
        {
            "sequence_org": "S", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167242687G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1476372356", 
                    "id": "rs1476372356", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs1476372356", 
                    "id": "rs1476372356", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
                "n-glyco-sequon-gain", 
                "o-glyco-site-loss"
            ], 
            "sequence_mut": "N", 
            "start_pos": 257, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 257, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (SVT->NVT)."
        }, 
        {
            "sequence_org": "I", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "C", 
            "chr_pos": "167250481T>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs748516497", 
                    "id": "rs748516497", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs748516497", 
                    "id": "rs748516497", 
                    "database": "ExAC"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs748516497", 
                    "id": "rs748516497", 
                    "database": "gnomAD"
                }
            ], 
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                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "T", 
            "start_pos": 2808, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 2808, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NTI->NTT)."
        }, 
        {
            "sequence_org": "I", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "C", 
            "chr_pos": "167250481T>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs748516497", 
                    "id": "rs748516497", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs748516497", 
                    "id": "rs748516497", 
                    "database": "ExAC"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs748516497", 
                    "id": "rs748516497", 
                    "database": "gnomAD"
                }
            ], 
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                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "T", 
            "start_pos": 2855, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 2855, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NII->NIT)."
        }, 
        {
            "sequence_org": "I", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "C", 
            "chr_pos": "167250613T>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1390145045", 
                    "id": "rs1390145045", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs1390145045#frequency_tab", 
                    "id": "rs1390145045", 
                    "database": "TOPMed"
                }
            ], 
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                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "T", 
            "start_pos": 2899, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 2899, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NKI->NKT)."
        }, 
        {
            "sequence_org": "D", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167242785G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs578201875", 
                    "id": "rs578201875", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs578201875", 
                    "id": "rs578201875", 
                    "database": "1000Genomes"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs578201875", 
                    "id": "rs578201875", 
                    "database": "ExAC"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs578201875", 
                    "id": "rs578201875", 
                    "database": "gnomAD"
                }
            ], 
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                "n-glyco-sequon-gain"
            ], 
            "sequence_mut": "N", 
            "start_pos": 290, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 290, 
            "minor_allelic_frequency": "0.0002", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (DVT->NVT)."
        }, 
        {
            "sequence_org": "D", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167250705G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs369944055", 
                    "id": "rs369944055", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs369944055", 
                    "id": "rs369944055", 
                    "database": "ExAC"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs369944055#frequency_tab", 
                    "id": "rs369944055", 
                    "database": "TOPMed"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs369944055", 
                    "id": "rs369944055", 
                    "database": "gnomAD"
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                "n-glyco-sequon-gain"
            ], 
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            "start_pos": 2930, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 2930, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (DDS->NDS)."
        }, 
        {
            "sequence_org": "P", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167250720C>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772409988", 
                    "id": "rs772409988", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772409988", 
                    "id": "rs772409988", 
                    "database": "ExAC"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs772409988", 
                    "id": "rs772409988", 
                    "database": "gnomAD"
                }
            ], 
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                "n-glyco-sequon-gain"
            ], 
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            "start_pos": 2935, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 2935, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NIP->NIT)."
        }, 
        {
            "sequence_org": "P", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "T", 
            "chr_pos": "167250798C>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1204907454", 
                    "id": "rs1204907454", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs1204907454", 
                    "id": "rs1204907454", 
                    "database": "gnomAD"
                }
            ], 
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                "n-glyco-sequon-gain"
            ], 
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            "start_pos": 2961, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 2961, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NPT->NST)."
        }, 
        {
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            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167250951G>", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs759414498", 
                    "id": "rs759414498", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs759414498", 
                    "id": "rs759414498", 
                    "database": "ExAC"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs759414498", 
                    "id": "rs759414498", 
                    "database": "gnomAD"
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            ], 
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                "germline"
            ], 
            "end_pos": 3012, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (DTT->NTT)."
        }, 
        {
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            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "C", 
            "chr_pos": "167250965G>", 
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                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs750604401", 
                    "id": "rs750604401", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs750604401", 
                    "id": "rs750604401", 
                    "database": "ExAC"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs750604401", 
                    "id": "rs750604401", 
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            ], 
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                "o-glyco-site-loss"
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                "germline"
            ], 
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            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (KLS->NLS)."
        }, 
        {
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            "chr_pos": "167251022G>", 
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                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772147805", 
                    "id": "rs772147805", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772147805", 
                    "id": "rs772147805", 
                    "database": "ExAC"
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                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs772147805#frequency_tab", 
                    "id": "rs772147805", 
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                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs772147805", 
                    "id": "rs772147805", 
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                "o-glyco-site-loss"
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                "ebi", 
                "germline"
            ], 
            "end_pos": 3035, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (KRS->NRS)."
        }, 
        {
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            "chr_id": "2", 
            "ref_nt": "G", 
            "chr_pos": "167251126A>", 
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                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs753011688", 
                    "id": "rs753011688", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs753011688", 
                    "id": "rs753011688", 
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                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs753011688", 
                    "id": "rs753011688", 
                    "database": "gnomAD"
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            ], 
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                "germline"
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            "end_pos": 3070, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NIN->NIS)."
        }, 
        {
            "sequence_org": "N", 
            "alt_nt": "null", 
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            "ref_nt": "G", 
            "chr_pos": "167251480A>", 
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                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs201465371", 
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                    "database": "dbSNP"
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                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs201465371", 
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                    "database": "ExAC"
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                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs201465371#frequency_tab", 
                    "id": "rs201465371", 
                    "database": "TOPMed"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs201465371", 
                    "id": "rs201465371", 
                    "database": "gnomAD"
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            ], 
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                "n-glyco-sequon-gain"
            ], 
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            "start_pos": 3188, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 3188, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NHN->NHS)."
        }, 
        {
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                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780204713", 
                    "id": "rs780204713", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780204713", 
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                {
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                    "id": "rs780204713", 
                    "database": "gnomAD"
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            ], 
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                "ebi", 
                "germline"
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            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (SRT->NRT)."
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                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs754083248", 
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                {
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            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (KTS->NTS)."
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        {
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            "alt_nt": "null", 
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            "chr_pos": "167254065C>", 
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                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs778880878", 
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                    "database": "dbSNP"
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                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs778880878", 
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                    "database": "ExAC"
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                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs778880878", 
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                "o-glyco-site-loss"
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                "germline"
            ], 
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            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (TLS->NLS)."
        }, 
        {
            "sequence_org": "S", 
            "alt_nt": "null", 
            "chr_id": "2", 
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            "chr_pos": "167243434G>", 
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                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1279959026", 
                    "id": "rs1279959026", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs1279959026#frequency_tab", 
                    "id": "rs1279959026", 
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                "o-glyco-site-loss"
            ], 
            "sequence_mut": "N", 
            "start_pos": 459, 
            "keywords": [
                "ebi", 
                "germline"
            ], 
            "end_pos": 459, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (SDT->NDT)."
        }, 
        {
            "sequence_org": "T", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
            "chr_pos": "167243428C>", 
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                {
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1476250386", 
                    "id": "rs1476250386", 
                    "database": "dbSNP"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs1476250386", 
                    "id": "rs1476250386", 
                    "database": "gnomAD"
                }
            ], 
            "glycoeffect": [
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                "o-glyco-site-loss"
            ], 
            "sequence_mut": "N", 
            "start_pos": 504, 
            "keywords": [
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                "germline"
            ], 
            "end_pos": 504, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (TIS->NIS)."
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        {
            "sequence_org": "M", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "C", 
            "chr_pos": "167218170T>", 
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                    "database": "dbSNP"
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                {
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                    "database": "TOPMed"
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            ], 
            "glycoeffect": [
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            "sequence_mut": "T", 
            "start_pos": 68, 
            "keywords": [
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            ], 
            "end_pos": 68, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NMM->NMT)."
        }, 
        {
            "sequence_org": "S", 
            "alt_nt": "null", 
            "chr_id": "2", 
            "ref_nt": "A", 
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                {
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs886564524#frequency_tab", 
                    "id": "rs886564524", 
                    "database": "TOPMed"
                }, 
                {
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs886564524", 
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                    "database": "gnomAD"
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            ], 
            "glycoeffect": [
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                "o-glyco-site-loss"
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            "sequence_mut": "N", 
            "start_pos": 903, 
            "keywords": [
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                "germline"
            ], 
            "end_pos": 903, 
            "minor_allelic_frequency": "", 
            "annotation": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (SKT->NKT)."
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            "name": "isoformset.uniprotkb", 
            "label": "Isoforms"
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        {
            "name": "homologset.mgi", 
            "label": "MGI Homologs"
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    ], 
    "refseq": {
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        "ac": "NP_001073278.1", 
        "name": "xin actin-binding repeat-containing protein 2 isoform 2", 
        "summary": ""
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            "annotation": "n_glycosylation_sequon", 
            "start_pos": 1031
        }, 
        {
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            "annotation": "n_glycosylation_sequon", 
            "start_pos": 107
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        {
            "end_pos": 1190, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 1188
        }, 
        {
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            "annotation": "n_glycosylation_sequon", 
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        {
            "end_pos": 1365, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 1363
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        {
            "end_pos": 1461, 
            "annotation": "n_glycosylation_sequon", 
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        }, 
        {
            "end_pos": 1469, 
            "annotation": "n_glycosylation_sequon", 
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        {
            "end_pos": 1515, 
            "annotation": "n_glycosylation_sequon", 
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        {
            "end_pos": 1593, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 1591
        }, 
        {
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            "annotation": "n_glycosylation_sequon", 
            "start_pos": 1917
        }, 
        {
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            "annotation": "n_glycosylation_sequon", 
            "start_pos": 2046
        }, 
        {
            "end_pos": 2085, 
            "annotation": "n_glycosylation_sequon", 
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        {
            "end_pos": 2128, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 2126
        }, 
        {
            "end_pos": 2550, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 2548
        }, 
        {
            "end_pos": 2673, 
            "annotation": "n_glycosylation_sequon", 
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        }, 
        {
            "end_pos": 269, 
            "annotation": "n_glycosylation_sequon", 
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        }, 
        {
            "end_pos": 2750, 
            "annotation": "n_glycosylation_sequon", 
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        {
            "end_pos": 2796, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 2794
        }, 
        {
            "end_pos": 2996, 
            "annotation": "n_glycosylation_sequon", 
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        {
            "end_pos": 3105, 
            "annotation": "n_glycosylation_sequon", 
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        {
            "end_pos": 3143, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 3141
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        {
            "end_pos": 3210, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 3208
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        {
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        {
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            "annotation": "n_glycosylation_sequon", 
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        {
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            "annotation": "n_glycosylation_sequon", 
            "start_pos": 772
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        {
            "end_pos": 806, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 804
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    ], 
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        {
            "url": "https://bgee.org/?page=gene&gene_id=ENSG00000163092", 
            "id": "ENSG00000163092", 
            "database": "Bgee"
        }, 
        {
            "url": "https://hive.biochemistry.gwu.edu/biomuta/proteinview/A4UGR9", 
            "id": "A4UGR9", 
            "database": "BioMuta"
        }, 
        {
            "url": "http://www.genecards.org/cgi-bin/carddisp.pl?gene=XIRP2", 
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            "database": "GeneCards"
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        {
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            "id": "129446", 
            "database": "GeneID"
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        {
            "url": "https://www.genenames.org/cgi-bin/gene_symbol_report?hgnc_id=14303", 
            "id": "14303", 
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        {
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            "id": "A4UGR9", 
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        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR001781", 
            "id": "IPR001781", 
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        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR012510", 
            "id": "IPR012510", 
            "database": "InterPro"
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        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR030072", 
            "id": "IPR030072", 
            "database": "InterPro"
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        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR030107", 
            "id": "IPR030107", 
            "database": "InterPro"
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        {
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+hsa:129446", 
            "id": "hsa:129446", 
            "database": "KEGG Pathway"
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        {
            "url": "http://www.omim.org/entry/609778", 
            "id": "609778", 
            "database": "MIM"
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        {
            "url": "https://www.nextprot.org/entry/NX_A4UGR9", 
            "id": "NX_A4UGR9", 
            "database": "neXtProt"
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        {
            "url": "https://www.oglcnac.mcw.edu/search/?query_protein=A4UGR9", 
            "id": "A4UGR9", 
            "database": "O-GlcNAc Database"
        }, 
        {
            "url": "https://omabrowser.org/oma/group/PPLMMLP/", 
            "id": "PPLMMLP", 
            "database": "OMA"
        }, 
        {
            "url": "http://www.orthodb.org/?query=30028at2759", 
            "id": "30028at2759", 
            "database": "OrthoDB"
        }, 
        {
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR22591", 
            "id": "PTHR22591", 
            "database": "PANTHER"
        }, 
        {
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR22591:SF1", 
            "id": "PTHR22591:SF1", 
            "database": "PANTHER"
        }, 
        {
            "url": "https://www.rcsb.org/structure/4F14", 
            "id": "4F14", 
            "database": "PDB"
        }, 
        {
            "url": "http://pfam.xfam.org/family/PF00412", 
            "id": "PF00412", 
            "database": "Pfam"
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        {
            "url": "http://pfam.xfam.org/family/PF08043", 
            "id": "PF08043", 
            "database": "Pfam"
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        {
            "url": "https://pharos.nih.gov/targets/A4UGR9", 
            "id": "A4UGR9", 
            "database": "PHAROS"
        }, 
        {
            "url": "http://purl.obolibrary.org/obo/PR_PR_A4UGR9", 
            "id": "PR_A4UGR9", 
            "database": "PRO"
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        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278", 
            "id": "NP_001073278", 
            "database": "RefSeq"
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001073278.1", 
            "id": "NP_001073278.1", 
            "database": "RefSeq"
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        {
            "url": "https://www.uniprot.org/uniprot/A0A0A0MQZ3", 
            "id": "A0A0A0MQZ3", 
            "database": "UniProtKB"
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        {
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            "id": "A0A0A0MQZ3-1", 
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        {
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            "id": "A0A5F9ZH43", 
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        {
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        {
            "url": "https://www.uniprot.org/uniprot/A0A5F9ZHW6", 
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        {
            "url": "https://www.uniprot.org/uniprot/A0A5F9ZHW6-1", 
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        {
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        {
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        {
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        {
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        {
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        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                            "resource": "Disease Ontology", 
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                        {
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                            "description": "", 
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                        {
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                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012094", 
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                            "description": "", 
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                            "id": "MONDO:0012094"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012094", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, type 4", 
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                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012094", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, on chromosome 7", 
                            "id": "MONDO:0012094"
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                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012741", 
                            "resource": "MONDO", 
                            "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene.", 
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                            "id": "MONDO:0012741"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012741", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "EHBP1 familial prostate cancer", 
                            "id": "MONDO:0012741"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012741", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 12; HPC12", 
                            "id": "MONDO:0012741"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012741", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "familial prostate cancer caused by mutation in EHBP1", 
                            "id": "MONDO:0012741"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012741", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, type 12", 
                            "id": "MONDO:0012741"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012741", 
                            "resource": "MONDO", 
                            "description": "", 
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                            "id": "MONDO:0012741"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012741", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 12", 
                            "id": "MONDO:0012741"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012244", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 5", 
                            "id": "MONDO:0012244"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012244", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 5", 
                            "id": "MONDO:0012244"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012244", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC5", 
                            "id": "MONDO:0012244"
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                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012244", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, type 5", 
                            "id": "MONDO:0012244"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012093", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 3", 
                            "id": "MONDO:0012093"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012093", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, type 3", 
                            "id": "MONDO:0012093"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012093", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC3", 
                            "id": "MONDO:0012093"
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                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012093", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 3", 
                            "id": "MONDO:0012093"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012758", 
                            "resource": "MONDO", 
                            "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene.", 
                            "name": "prostate cancer, hereditary, 13", 
                            "id": "MONDO:0012758"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012758", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 13; HPC13", 
                            "id": "MONDO:0012758"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012758", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "MSMB familial prostate cancer", 
                            "id": "MONDO:0012758"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012758", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC13", 
                            "id": "MONDO:0012758"
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                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012758", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, type 13", 
                            "id": "MONDO:0012758"
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                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012758", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 13", 
                            "id": "MONDO:0012758"
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                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012758", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "familial prostate cancer caused by mutation in MSMB", 
                            "id": "MONDO:0012758"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0011270", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 8", 
                            "id": "MONDO:0011270"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0011270", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, type 8", 
                            "id": "MONDO:0011270"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0011270", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 8", 
                            "id": "MONDO:0011270"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0011270", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "predisposing for prostate cancer", 
                            "id": "MONDO:0011270"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0011270", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC8", 
                            "id": "MONDO:0011270"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012300", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 6", 
                            "id": "MONDO:0012300"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012300", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 6", 
                            "id": "MONDO:0012300"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012300", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, type 6", 
                            "id": "MONDO:0012300"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012300", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC6", 
                            "id": "MONDO:0012300"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012597", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 9", 
                            "id": "MONDO:0012597"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012597", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC9", 
                            "id": "MONDO:0012597"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012597", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, type 9", 
                            "id": "MONDO:0012597"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012597", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 9", 
                            "id": "MONDO:0012597"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122", 
                            "resource": "MONDO", 
                            "description": "Prostate carcinoma that has developed in relatives of patients with a history of prostate carcinoma.", 
                            "name": "familial prostate carcinoma", 
                            "id": "MONDO:0023122"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "hereditary prostate cancer", 
                            "id": "MONDO:0023122"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "familial prostate cancer", 
                            "id": "MONDO:0023122"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary", 
                            "id": "MONDO:0023122"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, familial", 
                            "id": "MONDO:0023122"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "hereditary prostate carcinoma", 
                            "id": "MONDO:0023122"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012470", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC7", 
                            "id": "MONDO:0012470"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012470", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC7", 
                            "id": "MONDO:0012470"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012470", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer aggressiveness", 
                            "id": "MONDO:0012470"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012470", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 7", 
                            "id": "MONDO:0012470"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012470", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 7; HPC7", 
                            "id": "MONDO:0012470"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0011098", 
                            "resource": "MONDO", 
                            "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the RNASEL gene.", 
                            "name": "prostate cancer, hereditary, 1", 
                            "id": "MONDO:0011098"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0011098", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, type 1", 
                            "id": "MONDO:0011098"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0011098", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC1", 
                            "id": "MONDO:0011098"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0011098", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 1", 
                            "id": "MONDO:0011098"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0011098", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "familial prostate cancer caused by mutation in RNASEL", 
                            "id": "MONDO:0011098"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0011098", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "RNASEL familial prostate cancer", 
                            "id": "MONDO:0011098"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0011098", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 1; HPC1", 
                            "id": "MONDO:0011098"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0011098", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "Prca1", 
                            "id": "MONDO:0011098"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012768", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC11", 
                            "id": "MONDO:0012768"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012768", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 11", 
                            "id": "MONDO:0012768"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012768", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC11", 
                            "id": "MONDO:0012768"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012768", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 11; HPC11", 
                            "id": "MONDO:0012768"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012769", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC14", 
                            "id": "MONDO:0012769"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012769", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC14", 
                            "id": "MONDO:0012769"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012769", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 14; HPC14", 
                            "id": "MONDO:0012769"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012769", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 14", 
                            "id": "MONDO:0012769"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012770", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC15", 
                            "id": "MONDO:0012770"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012770", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC15", 
                            "id": "MONDO:0012770"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012770", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 15", 
                            "id": "MONDO:0012770"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012770", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 15; HPC15", 
                            "id": "MONDO:0012770"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0010257", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPCX1", 
                            "id": "MONDO:0010257"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0010257", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, X-linked 1", 
                            "id": "MONDO:0010257"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0010257", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer susceptibility, X-linked", 
                            "id": "MONDO:0010257"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0010257", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, X-linked 1; HPCX1", 
                            "id": "MONDO:0010257"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0010257", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPCX1", 
                            "id": "MONDO:0010257"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0010405", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPCX2", 
                            "id": "MONDO:0010405"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0010405", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, X-linked 2", 
                            "id": "MONDO:0010405"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0010405", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, X-linked 2; HPCX2", 
                            "id": "MONDO:0010405"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0010405", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPCX2", 
                            "id": "MONDO:0010405"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012620", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC10", 
                            "id": "MONDO:0012620"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012620", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 10", 
                            "id": "MONDO:0012620"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012620", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "prostate cancer, hereditary, 10; HPC10", 
                            "id": "MONDO:0012620"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0012620", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "HPC10", 
                            "id": "MONDO:0012620"
                        }, 
                        {
                            "url": "https://www.omim.org/entry/611868", 
                            "resource": "MIM", 
                            "description": "Prostate cancer, hereditary, 12", 
                            "name": "Prostate cancer, hereditary, 12", 
                            "id": "MIM:611868"
                        }, 
                        {
                            "url": "https://www.omim.org/entry/611928", 
                            "resource": "MIM", 
                            "description": "Prostate cancer, hereditary, 13", 
                            "name": "Prostate cancer, hereditary, 13", 
                            "id": "MIM:611928"
                        }, 
                        {
                            "url": "https://www.omim.org/entry/176807", 
                            "resource": "MIM", 
                            "description": "Prostate cancer", 
                            "name": "Prostate cancer", 
                            "id": "MIM:176807"
                        }, 
                        {
                            "url": "https://www.omim.org/entry/601518", 
                            "resource": "MIM", 
                            "description": "Prostate cancer, hereditary, 1", 
                            "name": "Prostate cancer, hereditary, 1", 
                            "id": "MIM:601518"
                        }, 
                        {
                            "url": "https://www.omim.org/entry/611955", 
                            "resource": "MIM", 
                            "description": "Prostate cancer, hereditary, 11", 
                            "name": "Prostate cancer, hereditary, 11", 
                            "id": "MIM:611955"
                        }
                    ], 
                    "recommended_name": {
                        "url": "http://disease-ontology.org/term/DOID:10283", 
                        "resource": "Disease Ontology", 
                        "description": "A male reproductive organ cancer that is located_in the prostate.", 
                        "name": "prostate cancer", 
                        "id": "DOID:10283"
                    }
                }
            ], 
            "evidence": [
                {
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/A4UGR9", 
                    "id": "A4UGR9", 
                    "database": "BioXpress"
                }
            ], 
            "url": "http://disease-ontology.org/term/DOID:10283", 
            "significant": "Yes"
        }, 
        {
            "name": "Urinary bladder cancer [DO disease name]", 
            "trend": "Down", 
            "disease": [
                {
                    "disease_id": "DOID:11054", 
                    "synonyms": [
                        {
                            "url": "http://disease-ontology.org/term/DOID:11054", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "bladder cancer", 
                            "id": "DOID:11054"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:11054", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "tumor of the bladder", 
                            "id": "DOID:11054"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "A primary or metastatic malignant neoplasm involving the bladder.", 
                            "name": "urinary bladder cancer", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "urinary bladder malignant neoplasm", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant tumor of bladder", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant tumor, urinary bladder", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant neoplasm of the bladder", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant urinary bladder tumor", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant neoplasm of the urinary bladder", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "bladder cancer", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant tumor of the urinary bladder", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant urinary bladder neoplasm", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant neoplasm, bladder", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "urinary bladder malignant tumor", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant bladder tumor", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant neoplasm, urinary bladder", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "urinary bladder cancer", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant tumor of the bladder", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant bladder neoplasm", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "tumor of the bladder", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant neoplasm of urinary bladder", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant neoplasm of bladder", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "cancer of urinary bladder", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant tumor of urinary bladder", 
                            "id": "MONDO:0001187"
                        }, 
                        {
                            "url": "https://www.omim.org/entry/109800", 
                            "resource": "MIM", 
                            "description": "Bladder cancer", 
                            "name": "Bladder cancer", 
                            "id": "MIM:109800"
                        }
                    ], 
                    "recommended_name": {
                        "url": "http://disease-ontology.org/term/DOID:11054", 
                        "resource": "Disease Ontology", 
                        "description": "An urinary system cancer that results_in malignant growth located_in the urinary bladder.", 
                        "name": "urinary bladder cancer", 
                        "id": "DOID:11054"
                    }
                }
            ], 
            "evidence": [
                {
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/A4UGR9", 
                    "id": "A4UGR9", 
                    "database": "BioXpress"
                }
            ], 
            "url": "http://disease-ontology.org/term/DOID:11054", 
            "significant": "No"
        }, 
        {
            "name": "Thyroid gland cancer [DO disease name]", 
            "trend": "Down", 
            "disease": [
                {
                    "disease_id": "DOID:1781", 
                    "synonyms": [
                        {
                            "url": "http://disease-ontology.org/term/DOID:1781", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "neoplasm of thyroid gland", 
                            "id": "DOID:1781"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:1781", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant neoplasm of thyroid gland", 
                            "id": "DOID:1781"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:1781", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant tumour of thyroid gland", 
                            "id": "DOID:1781"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:1781", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "Thyroid gland neoplasm", 
                            "id": "DOID:1781"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:1781", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "thyroid neoplasm", 
                            "id": "DOID:1781"
                        }
                    ], 
                    "recommended_name": {
                        "url": "http://disease-ontology.org/term/DOID:1781", 
                        "resource": "Disease Ontology", 
                        "description": "An endocrine gland cancer located in the thryoid gland located in the neck below the thyroid cartilage.", 
                        "name": "thyroid gland cancer", 
                        "id": "DOID:1781"
                    }
                }
            ], 
            "evidence": [
                {
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/A4UGR9", 
                    "id": "A4UGR9", 
                    "database": "BioXpress"
                }
            ], 
            "url": "http://disease-ontology.org/term/DOID:1781", 
            "significant": "Yes"
        }, 
        {
            "name": "Liver cancer [DO disease name]", 
            "trend": "Down", 
            "disease": [
                {
                    "disease_id": "DOID:3571", 
                    "synonyms": [
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "primary malignant neoplasm of liver", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant neoplasm of liver", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "resectable malignant neoplasm of the liver", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant neoplasm of liver, primary", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "Ca liver - primary", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "neoplasm of liver", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant tumor of liver", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "primary malignant neoplasm of Liver", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "Resectable malignant neoplasm of Liver", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant neoplasm of liver, not specified as primary or secondary", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "ca liver - primary", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "non-resectable primary hepatic malignant neoplasm", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "primary liver cancer", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "hepatic neoplasm", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant hepato-biliary neoplasm", 
                            "id": "DOID:3571"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3571", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "hepatic cancer", 
                            "id": "DOID:3571"
                        }
                    ], 
                    "recommended_name": {
                        "url": "http://disease-ontology.org/term/DOID:3571", 
                        "resource": "Disease Ontology", 
                        "description": "A hepatobiliary system cancer that is located_in the liver.", 
                        "name": "liver cancer", 
                        "id": "DOID:3571"
                    }
                }
            ], 
            "evidence": [
                {
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/A4UGR9", 
                    "id": "A4UGR9", 
                    "database": "BioXpress"
                }
            ], 
            "url": "http://disease-ontology.org/term/DOID:3571", 
            "significant": "No"
        }, 
        {
            "name": "Lung squamous cell carcinoma [DO disease name]", 
            "trend": "Down", 
            "disease": [
                {
                    "disease_id": "DOID:3907", 
                    "synonyms": [
                        {
                            "url": "http://disease-ontology.org/term/DOID:3907", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "Epidermoid cell carcinoma of the lung", 
                            "id": "DOID:3907"
                        }
                    ], 
                    "recommended_name": {
                        "url": "http://disease-ontology.org/term/DOID:3907", 
                        "resource": "Disease Ontology", 
                        "description": "A non-small cell lung carcinoma that has_material_basis_in the squamous cell.", 
                        "name": "lung squamous cell carcinoma", 
                        "id": "DOID:3907"
                    }
                }
            ], 
            "evidence": [
                {
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/A4UGR9", 
                    "id": "A4UGR9", 
                    "database": "BioXpress"
                }
            ], 
            "url": "http://disease-ontology.org/term/DOID:3907", 
            "significant": "Yes"
        }, 
        {
            "name": "Lung adenocarcinoma [DO disease name]", 
            "trend": "Up", 
            "disease": [
                {
                    "disease_id": "DOID:3910", 
                    "synonyms": [
                        {
                            "url": "http://disease-ontology.org/term/DOID:3910", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "nonsmall cell adenocarcinoma", 
                            "id": "DOID:3910"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:3910", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "bronchogenic lung adenocarcinoma", 
                            "id": "DOID:3910"
                        }
                    ], 
                    "recommended_name": {
                        "url": "http://disease-ontology.org/term/DOID:3910", 
                        "resource": "Disease Ontology", 
                        "description": "A lung cancer that derives_from epithelial cells of glandular origin.", 
                        "name": "lung adenocarcinoma", 
                        "id": "DOID:3910"
                    }
                }
            ], 
            "evidence": [
                {
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/A4UGR9", 
                    "id": "A4UGR9", 
                    "database": "BioXpress"
                }
            ], 
            "url": "http://disease-ontology.org/term/DOID:3910", 
            "significant": "No"
        }, 
        {
            "name": "Esophageal cancer [DO disease name]", 
            "trend": "Down", 
            "disease": [
                {
                    "disease_id": "DOID:5041", 
                    "synonyms": [
                        {
                            "url": "http://disease-ontology.org/term/DOID:5041", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "esophagus cancer", 
                            "id": "DOID:5041"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:5041", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant neoplasm of distal third of esophagus", 
                            "id": "DOID:5041"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:5041", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "Ca middle third oesophagus", 
                            "id": "DOID:5041"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:5041", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant tumor of Distal Third of esophagus", 
                            "id": "DOID:5041"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:5041", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant tumor of abdominal esophagus", 
                            "id": "DOID:5041"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:5041", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant tumor of Proximal Third of esophagus", 
                            "id": "DOID:5041"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:5041", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant neoplasm of proximal third of esophagus", 
                            "id": "DOID:5041"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:5041", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant neoplasm of middle third of oesophagus", 
                            "id": "DOID:5041"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:5041", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant neoplasm of upper third esophagus", 
                            "id": "DOID:5041"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:5041", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant tumor of the middle Third of the esophagus", 
                            "id": "DOID:5041"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:5041", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "Ca lower third oesophagus", 
                            "id": "DOID:5041"
                        }, 
                        {
                            "url": "http://disease-ontology.org/term/DOID:5041", 
                            "resource": "Disease Ontology", 
                            "description": "", 
                            "name": "malignant neoplasm of lower third of oesophagus", 
                            "id": "DOID:5041"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "A primary or metastatic malignant neoplasm involving the esophagus.", 
                            "name": "esophageal cancer", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant tumor of abdominal esophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant tumor of proximal third of esophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "gastric cardia adenocarcinoma, susceptibility to", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "cancer of esophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant neoplasm of lower third of oesophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "Escc, susceptibility to", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant neoplasm of upper third esophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant tumor of distal third of esophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "Aerodigestive tract cancer, susceptibility to", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant neoplasm of middle third of oesophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "esophageal cancer", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant neoplasm of esophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant neoplasm of proximal third of esophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant neoplasm of the esophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant tumor of esophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant esophageal tumor", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "Ca lower third oesophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant tumor of the middle third of the esophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant esophageal neoplasm", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant esophagus neoplasm", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant esophagus tumor", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "esophagus cancer", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant neoplasm of distal third of esophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "Ca middle third oesophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "malignant tumor of the esophagus", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://monarchinitiative.org/disease/MONDO:0007576", 
                            "resource": "MONDO", 
                            "description": "", 
                            "name": "esophageal squamous cell carcinoma, susceptibility to", 
                            "id": "MONDO:0007576"
                        }, 
                        {
                            "url": "https://www.omim.org/entry/133239", 
                            "resource": "MIM", 
                            "description": "Esophageal cancer", 
                            "name": "Esophageal cancer", 
                            "id": "MIM:133239"
                        }
                    ], 
                    "recommended_name": {
                        "url": "http://disease-ontology.org/term/DOID:5041", 
                        "resource": "Disease Ontology", 
                        "description": "A gastrointestinal system cancer that is located_in the esophagus.", 
                        "name": "esophageal cancer", 
                        "id": "DOID:5041"
                    }
                }
            ], 
            "evidence": [
                {
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/A4UGR9", 
                    "id": "A4UGR9", 
                    "database": "BioXpress"
                }
            ], 
            "url": "http://disease-ontology.org/term/DOID:5041", 
            "significant": "No"
        }
    ], 
    "glycosylation": [
        {
            "residue": "Thr", 
            "site_category": "reported_with_glycan", 
            "end_pos": 2838, 
            "evidence": [
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                }, 
                {
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    "disease": [], 
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            ], 
            "start_pos": 1989, 
            "end_pos": 1989, 
            "kinase_uniprot_canonical_ac": ""
        }, 
        {
            "residue": "Ser", 
            "kinase_gene_name": "", 
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            ], 
            "start_pos": 1994, 
            "end_pos": 1994, 
            "kinase_uniprot_canonical_ac": ""
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        {
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}
