{
    "uniprot_canonical_ac": "A0A0G2JZ84-1",
    "uniprot_ac": "A0A0G2JZ84",
    "uniprot_id": "A0A0G2JZ84_RAT",
    "mass": {
        "chemical_mass": 291350.0,
        "monoisotopic_mass": 291350.0
    },
    "refseq": {},
    "gene_names": [
        {
            "name": "Epg5",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JZ84",
            "id": "A0A0G2JZ84"
        }
    ],
    "protein_names": [
        {
            "name": "Ectopic P-granules autophagy protein 5 homolog",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A0G2JZ84"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0060356",
            "recommended_name": {
                "id": "DOID:0060356",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0060356",
                "name": "Vici syndrome",
                "description": "A syndrome characterized by callosal agenesis, cataracts, cardiomyopathy, combined immunodeficiency and hypopigmentation. It has_material_basis_in mutation in the EPG5 gene on chromosome 18q12.3."
            },
            "synonyms": [
                {
                    "id": "DOID:0060356",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060356",
                    "name": "immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum",
                    "description": ""
                },
                {
                    "id": "MONDO:0009452",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009452",
                    "name": "Vici syndrome",
                    "description": "A very rare and severe congenital multisystem disorder characterized by the principal features of agenesis of the corpus callosum, cataracts, oculocutaneous hypopigmentation, cardiomyopathy and combined immunodeficiency."
                },
                {
                    "id": "MONDO:0009452",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009452",
                    "name": "Dionisi-Vici-Sabetta-Gambarara syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0009452",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009452",
                    "name": "Vici syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0009452",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009452",
                    "name": "absent corpus callosum-cataract-immunodeficiency syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0009452",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009452",
                    "name": "corpus callosum agenesis-cataract-immunodeficiency syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0009452",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009452",
                    "name": "immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum",
                    "description": ""
                },
                {
                    "id": "MONDO:0009452",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009452",
                    "name": "Dionisi Vici Sabetta Gambarara syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0009452",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009452",
                    "name": "VICIS",
                    "description": ""
                },
                {
                    "id": "MONDO:0009452",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009452",
                    "name": "absent corpus callosum cataract immunodeficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009452",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009452",
                    "name": "immunodeficiency with cleft Lip/palate, cataract, hypopigmentation, and absent corpus callosum",
                    "description": ""
                },
                {
                    "id": "MONDO:0009452",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009452",
                    "name": "immunodeficiency with cleft lip/palate, cataract, hypopigmentation and absent corpus callosum",
                    "description": ""
                },
                {
                    "id": "MIM:242840",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/242840",
                    "name": "Vici syndrome",
                    "description": "Vici syndrome"
                }
            ],
            "evidence": [
                {
                    "id": "0060356",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0060356"
                }
            ]
        },
        {
            "disease_id": "DOID:10584",
            "recommended_name": {
                "id": "DOID:10584",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:10584",
                "name": "retinitis pigmentosa",
                "description": "A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss."
            },
            "synonyms": [
                {
                    "id": "DOID:10584",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10584",
                    "name": "pericentral pigmentary retinopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0019200",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0019200",
                    "name": "retinitis pigmentosa",
                    "description": "Retinitis pigmentosa (RP) is an inherited retinal dystrophy leading to progressive loss of the photoreceptors and retinal pigment epithelium and resulting in blindness usually after several decades."
                },
                {
                    "id": "MONDO:0019200",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0019200",
                    "name": "retinitis pigmentosa",
                    "description": ""
                },
                {
                    "id": "MONDO:0019200",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0019200",
                    "name": "pericentral pigmentary retinopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0019200",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0019200",
                    "name": "Rod-cone dystrophy",
                    "description": ""
                },
                {
                    "id": "MIM:268000",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/268000",
                    "name": "Retinitis pigmentosa",
                    "description": "Retinitis pigmentosa"
                }
            ],
            "evidence": [
                {
                    "id": "10584",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:10584"
                }
            ]
        },
        {
            "disease_id": "DOID:332",
            "recommended_name": {
                "id": "DOID:332",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:332",
                "name": "amyotrophic lateral sclerosis",
                "description": "A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing."
            },
            "synonyms": [
                {
                    "id": "DOID:332",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:332",
                    "name": "ALS",
                    "description": ""
                },
                {
                    "id": "DOID:332",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:332",
                    "name": "Lou Gehrig's disease",
                    "description": ""
                },
                {
                    "id": "DOID:332",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:332",
                    "name": "motor neuron disease, bulbar",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "ALS1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "FALS",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1, autosomal dominant amyotrophic lateral sclerosis 1, autosomal recessive, included",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1, familial",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, familial",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, sporadic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, sporadic, included",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MIM:105400",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/105400",
                    "name": "Amyotrophic lateral sclerosis 1",
                    "description": "Amyotrophic lateral sclerosis 1"
                }
            ],
            "evidence": [
                {
                    "id": "332",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:332"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Rattus norvegicus",
            "taxid": 10116,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0G2JZ84",
                    "url": "https://www.uniprot.org/uniprot/A0A0G2JZ84"
                }
            ],
            "common_name": "Rat"
        }
    ],
    "gene": [
        {
            "name": "Epg5",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JZ84",
            "locus": {
                "chromosome": "18",
                "start_pos": 71501502,
                "end_pos": 71404010,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "ENSRNOG00000052894",
                        "url": "https://www.ensembl.org/id/ENSRNOG00000052894"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "ENSRNOG00000052894",
            "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000052894",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "364902",
            "url": "https://www.ncbi.nlm.nih.gov/gene/364902",
            "database": "GeneID",
            "categories": [
                "Genome Annotation"
            ]
        },
        {
            "id": "rno:364902",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:364902",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "EHFLPMY",
            "url": "https://omabrowser.org/oma/group/EHFLPMY/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "2907346at2759",
            "url": "http://www.orthodb.org/?query=2907346at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR31139",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR31139",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR31139:SF4",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR31139:SF4",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "XP_006222699",
            "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006222699",
            "database": "RefSeq",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "1306286",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1306286",
            "database": "RGD",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "A0A0G2JZ84",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JZ84",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0G2JZ84-1",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JZ84-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I6ACL1",
            "url": "https://www.uniprot.org/uniprot/A0A8I6ACL1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I6ACL1-1",
            "url": "https://www.uniprot.org/uniprot/A0A8I6ACL1-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MAEAVKPRRAKAKASRTKGKEKKKHEALQSSDAALLSETCREQGILSPASELKGDGLNVSAASQFHSDVCGWNESEMFDIPLTSLTVVDEGPPIQDTEDLKDRGEVAARDGDDEIELKVDPGDNVRTEGDPGDPSKNFPEVEERTFMQCGSPENTLQSDFPCTQQEGASSQVRESPTRKEDAKALGCSTVLQDVSLHSPYETKEVPQPPRVKKLYPELPAEIAEVPSLVAVKPLLRSERLYPELPSQPELAPFTKEQLKLLEPGSWLENVESYVEEFDNIAHQDRHEFYELLLNYSRCRKQLLLAEAELLTLMSDCQNAKSRLWSFKDEQMAVQGICADQVKVYGHHHYQRVEMNENALGELKKLFDAKSEHLHQTLTLHSYTSVLSRLQVESYIYTLLNSSAVLRSVAVYQADKVSKLTESIPSDVCQLKECISVLFMFTRRVSEDAQFHEDILLWLQKLVSVLQRIGCPGDHFFLLNHILRCPAGISEWAVPFIQIKVLNNPSGVFHFMQSLALLMSPAKNRAEFMCHMKPSEWKPSSSGPASGNWTLVDEGGEEDEDPETSWSLLNEDDLVTLLSQFPFHELFQHLLGFKAKGDYLPETTRPQEMMKIFAFANSLVELLAVGLETFNRARYRQFVKRIGYLIRMTLGYVSDHWAQYVSHNTDVRLTLQPYSMEKLQIEFDELFLRAVLHVLKAKRLGIWLFMSEMPFGTLSVQMLWKLFYLMHQVESGNLQQLCASLQPAECKRQLQDPEHVASFEKCLSSMNSSEEICLLTTFAQMARARRTNVDEGFIKIIVLEIYEVSYVILSTRETFSKVGRELLGSIAAVHPEIISVLLDRVQETIDQVGMVSLYLFKELPLHLWRPSASEIAVIRDWLLSYNLAAVKNKLACVILEGLNWGFAKQGNLHLDQALHTEVALLVLEAYQKYLAQKPYAGLISESMKQVSYLASIVRYGETPETSFNQWAWNLILRLKLHKNDFGRQNFPVVPFCNTVPDMTESSMFHPLLKAVKSGLPIGCYLALAVTAVGHSIEKFCAEGIPLLGVLVQSRHLRAVVHVLDKVLPVFYPCQYYLLKNEQFLSNLLLFLHLDSGVPQGVTQQVTHRVAHHLTGAIHGDNVKLLNSMIQAHICVSTQPDEVGPVAVLEFWVQALISQHLWYREQSILFLMDHLCKTAFQLMQEDCVQKLLYQQHKNALGYHCDRSLLSSLVNWIVAGNITPSFVEGLSTSTQVWFAWTVLNMESIFEEDSQLRRVVERELVINAFSPDQALKKAQVQLKLPIVPSLQRLLIYRWAHQALVTPADHPLLPLIWQKFFLLYLHRPGPQYGLPVDGCIGRRFFQSPSHVNLLKDMKRRLTEVADFHYAASKALRVPAEGSEGTPERQAGTPGFLTSPELHRELVRLFNVYILWLEDENFQKGDIYIPSLPKHYDVYRLAKVMQNQQDLWMEYANMERIQHEFQETVALWTQAKLESHSVPCSSSTQLDFTDPLLAKERVLSNLQRHEAPHPPLVLHPMRPPVPLISSAVLLAQKDATQLMCADLNLLQQQARTATLRESQQVALDGELLEAMPKQYVNREEQATLHLECRGSSGKKCQGAAVVTVQFEGMCKNEAISQQVHVLQKEVWQFQAEAAQPPALNVVEAAVHAENLITALVNTYKLQPTPGVQKVGISLFFTVVDYVSEETQRHPPTRQFFTSCIEILGQVFISGTKSECKKLLQTILKNRRLCSLLSPFFTPNAAPAEFIPLYEKVAKCLSEDNSDLVFMLLTKFDVQQWLSSTKPPLSDRTRLLESIHLALTAWGLEPEEDIMMPFNLFCKHWTHLLLYQFPDQYSDVLRLLVQSSAEQLLSPECWKATLKALGCYAPSIQQGEASVESSVLHSASDVLLSDKQVTETVQWLSDFFYKLRLSKLDFKSFGLFSKWSPYMADVKTFLGYLVKRLTDLELASLAQDPTASSKEVLRSLHSQIIQLFKPWILVLEDTESSHQRHYPWLESDTVVASSLVQLFTDCVSSLHASFKDKLLPGDEGALRLHLLHYTESCTAPRMPEFILYAFHSAYQKLEWKDLHPDQRLMEAFFKVERGSPKSCFLFLGSVLCRVNWVSVLSDAWSPSPLPETQSMVVCLLFMMVLLAKEAQLVDETDSPLLSLLGQTSSLSWHLVDFVSYQSVLGYFSSHYPPSVILAQDCSAELIVRLLKVSAGLSLPADSRKHVDIVPKCQAFTHQMAQFLSALEQDGKVAFPALGQEVSKLLDDIITFNPPDMDSQTRHMALSSLFMEVLMMMNSAAVPTAEYLGVSIRTWIGQKVHGLVVLPLLTAACQSLASVRHMAETTEACITAYFKESSLDQNLGWGPILVSLQVPELTMQEFLQECLALGSCLTLYVYLLQCLNSEQTVKNEMKVLLILSTWLEHVYPSSAQEEAKLLLWWHQALQLSLVQLEQDDSVLTESVIRILLMLQGRQSLMAEERLSSGILGAIGLGRKSPLSNRFRVVARSMAAFLSVQVPAEDQIRLKPSSELHLTPKAQQVLAALESMTLSKQYVEYQDQILHAVQFIRHPGHCLQNGKSFLAFFVNRLYPEVHYLDNIR",
        "length": 2575,
        "header": "tr|A0A0G2JZ84-1|A0A0G2JZ84_RAT Isoform 1 of Ectopic P-granules autophagy protein 5 homolog  OS=Rattus norvegicus OX=10116 GN=Epg5 PE=4 SV=1 CANONICAL=A0A0G2JZ84-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A0G2JZ84-1",
            "url": "",
            "sequence": {
                "sequence": "MAEAVKPRRAKAKASRTKGKEKKKHEALQSSDAALLSETCREQGILSPASELKGDGLNVSAASQFHSDVCGWNESEMFDIPLTSLTVVDEGPPIQDTEDLKDRGEVAARDGDDEIELKVDPGDNVRTEGDPGDPSKNFPEVEERTFMQCGSPENTLQSDFPCTQQEGASSQVRESPTRKEDAKALGCSTVLQDVSLHSPYETKEVPQPPRVKKLYPELPAEIAEVPSLVAVKPLLRSERLYPELPSQPELAPFTKEQLKLLEPGSWLENVESYVEEFDNIAHQDRHEFYELLLNYSRCRKQLLLAEAELLTLMSDCQNAKSRLWSFKDEQMAVQGICADQVKVYGHHHYQRVEMNENALGELKKLFDAKSEHLHQTLTLHSYTSVLSRLQVESYIYTLLNSSAVLRSVAVYQADKVSKLTESIPSDVCQLKECISVLFMFTRRVSEDAQFHEDILLWLQKLVSVLQRIGCPGDHFFLLNHILRCPAGISEWAVPFIQIKVLNNPSGVFHFMQSLALLMSPAKNRAEFMCHMKPSEWKPSSSGPASGNWTLVDEGGEEDEDPETSWSLLNEDDLVTLLSQFPFHELFQHLLGFKAKGDYLPETTRPQEMMKIFAFANSLVELLAVGLETFNRARYRQFVKRIGYLIRMTLGYVSDHWAQYVSHNTDVRLTLQPYSMEKLQIEFDELFLRAVLHVLKAKRLGIWLFMSEMPFGTLSVQMLWKLFYLMHQVESGNLQQLCASLQPAECKRQLQDPEHVASFEKCLSSMNSSEEICLLTTFAQMARARRTNVDEGFIKIIVLEIYEVSYVILSTRETFSKVGRELLGSIAAVHPEIISVLLDRVQETIDQVGMVSLYLFKELPLHLWRPSASEIAVIRDWLLSYNLAAVKNKLACVILEGLNWGFAKQGNLHLDQALHTEVALLVLEAYQKYLAQKPYAGLISESMKQVSYLASIVRYGETPETSFNQWAWNLILRLKLHKNDFGRQNFPVVPFCNTVPDMTESSMFHPLLKAVKSGLPIGCYLALAVTAVGHSIEKFCAEGIPLLGVLVQSRHLRAVVHVLDKVLPVFYPCQYYLLKNEQFLSNLLLFLHLDSGVPQGVTQQVTHRVAHHLTGAIHGDNVKLLNSMIQAHICVSTQPDEVGPVAVLEFWVQALISQHLWYREQSILFLMDHLCKTAFQLMQEDCVQKLLYQQHKNALGYHCDRSLLSSLVNWIVAGNITPSFVEGLSTSTQVWFAWTVLNMESIFEEDSQLRRVVERELVINAFSPDQALKKAQVQLKLPIVPSLQRLLIYRWAHQALVTPADHPLLPLIWQKFFLLYLHRPGPQYGLPVDGCIGRRFFQSPSHVNLLKDMKRRLTEVADFHYAASKALRVPAEGSEGTPERQAGTPGFLTSPELHRELVRLFNVYILWLEDENFQKGDIYIPSLPKHYDVYRLAKVMQNQQDLWMEYANMERIQHEFQETVALWTQAKLESHSVPCSSSTQLDFTDPLLAKERVLSNLQRHEAPHPPLVLHPMRPPVPLISSAVLLAQKDATQLMCADLNLLQQQARTATLRESQQVALDGELLEAMPKQYVNREEQATLHLECRGSSGKKCQGAAVVTVQFEGMCKNEAISQQVHVLQKEVWQFQAEAAQPPALNVVEAAVHAENLITALVNTYKLQPTPGVQKVGISLFFTVVDYVSEETQRHPPTRQFFTSCIEILGQVFISGTKSECKKLLQTILKNRRLCSLLSPFFTPNAAPAEFIPLYEKVAKCLSEDNSDLVFMLLTKFDVQQWLSSTKPPLSDRTRLLESIHLALTAWGLEPEEDIMMPFNLFCKHWTHLLLYQFPDQYSDVLRLLVQSSAEQLLSPECWKATLKALGCYAPSIQQGEASVESSVLHSASDVLLSDKQVTETVQWLSDFFYKLRLSKLDFKSFGLFSKWSPYMADVKTFLGYLVKRLTDLELASLAQDPTASSKEVLRSLHSQIIQLFKPWILVLEDTESSHQRHYPWLESDTVVASSLVQLFTDCVSSLHASFKDKLLPGDEGALRLHLLHYTESCTAPRMPEFILYAFHSAYQKLEWKDLHPDQRLMEAFFKVERGSPKSCFLFLGSVLCRVNWVSVLSDAWSPSPLPETQSMVVCLLFMMVLLAKEAQLVDETDSPLLSLLGQTSSLSWHLVDFVSYQSVLGYFSSHYPPSVILAQDCSAELIVRLLKVSAGLSLPADSRKHVDIVPKCQAFTHQMAQFLSALEQDGKVAFPALGQEVSKLLDDIITFNPPDMDSQTRHMALSSLFMEVLMMMNSAAVPTAEYLGVSIRTWIGQKVHGLVVLPLLTAACQSLASVRHMAETTEACITAYFKESSLDQNLGWGPILVSLQVPELTMQEFLQECLALGSCLTLYVYLLQCLNSEQTVKNEMKVLLILSTWLEHVYPSSAQEEAKLLLWWHQALQLSLVQLEQDDSVLTESVIRILLMLQGRQSLMAEERLSSGILGAIGLGRKSPLSNRFRVVARSMAAFLSVQVPAEDQIRLKPSSELHLTPKAQQVLAALESMTLSKQYVEYQDQILHAVQFIRHPGHCLQNGKSFLAFFVNRLYPEVHYLDNIR",
                "length": 2575,
                "header": "tr|A0A0G2JZ84-1|A0A0G2JZ84_RAT Isoform 1 of Ectopic P-granules autophagy protein 5 homolog  OS=Rattus norvegicus OX=10116 GN=Epg5 PE=4 SV=1 CANONICAL=A0A0G2JZ84-1"
            },
            "locus": {
                "chromosome": "18",
                "start_pos": 71499735,
                "end_pos": 71404083,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000078403.2",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000078403.2"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000070948.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000070948.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8I6ACL1-1",
            "url": "",
            "sequence": {
                "sequence": "MAEAVKPRRAKAKASRTKGKEKKKHEALQSSDAALLSETCREQGILSPASELKGDGLNVSAASQFHSDVCGWNESEMFDIPLTSLTVVDEGPPIQDTEDLKDRGEVAARDGDDEIELKVDPGDNVRTEGDPGDPSKNFPEVEERTFMQCGSPENTLQSDFPCTQQEGASSQVRESPTRKEDAKALGCSTVLQDVSLHSPYETKEVPQPPRVKKLYPELPAEIAEVPSLVAVKPLLRSERLYPELPSQPELAPFTKEQLKLLEPGSWLENVESYVEEFDNIAHQDRHEFYELLLNYSRCRKQLLLAEAELLTLMSDCQNAKSRLWSFKDEQMAVQGICADQVKVYGHHHYQRVEMNENALGELKKLFDAKSEHLHQTLTLHSYTSVLSRLQVESYIYTLLNSSAVLRSVAVYQADKDTPEEGIRSHYRVLADSIKVLNNPSGVFHFMQSLALLMSPAKNRAEFMCHMKPSEWKPSSSGPASGNWTLVDEGGEEDEDPETSWSLLNEDDLVTLLSQFPFHELFQHLLGFKAKGDYLPETTRPQEMMKIFAFANSLVELLAVGLETFNRARYRQFVKRIGYLIRMTLGYVSDHWAQYVSHNTDVRLTLQPYSMEKLQIEFDELFLRAVLHVLKAKRLGIWLFMSEMPFGTLSVQMLWKLFYLMHQVESGNLQQLCASLQPAECKRQLQDPEHVASFEKCLSSMNSSEEICLLTTFAQMARARRTNVDEGFIKIIVLEIYEVSYVILSTRETFSKVGRELLGSIAAVHPEIISVLLDRVQETIDQVGMVSLYLFKELPLHLWRPSASEIAVIRDWLLSYNLAAVKNKLACVILEGLNWGFAKQGNLHLDQALHTEVALLVLEAYQKYLAQKPYAGLISESMKQVSYLASIVRYGETPETSFNQWAWNLILRLKLHKNDFGRQNFPVVPFCNTVPDMTESSMFHPLLKAVKSGLPIGCYLALAVTAVGHSIEKFCAEGIPLLGVLVQSRHLRAVVHVLDKVLPVFYPCQYYLLKNEQFLSNLLLFLHLDSGVPQGVTQQVTHRVAHHLTGAIHGDNVKLLNSMIQAHICVSTQPDEVGPVAVLEFWVQALISQHLWYREQSILFLMDHLCKTAFQLMQEDCVQKLLYQQHKNALGYHCDRSLLSSLVNWIVAGNITPSFVEGLSTSTQVWFAWTVLNMESIFEEDSQLRRVVERELVINAFSPDQALKKAQVQLKLPIVPSLQRLLIYRWAHQALVTPADHPLLPLIWQKFFLLYLHRPGPQYGLPVDGCIGRRFFQSPSHVNLLKDMKRRLTEVADFHYAASKALRVPAEGSEGTPERQAGTPGFLTSPELHRELVRLFNVYILWLEDENFQKGDIYIPSLPKHYDVYRLAKVMQNQQDLWMEYANMERIQHEFQETVALWTQAKLESHSVPCSSSTQLDFTDPLLAKERVLSNLQRHEAPHPPLVLHPMRPPVPLISSAVLLAQKDATQLMCADLNLLQQQARTATLRESQQVALDGELLEAMPKQYVNREEQATLHLECRGSSGKKCQGAAVVTVQFEGMCKNEAISQQVHVLQKEVWQFQAEAAQPPALNVVEAAVHAENLITALVNTYKLQPTPGVQKVGISLFFTVVDYVSEETQRHPPTRQFFTSCIEILGQVFISGTKSECKKLLQTILKNRRLCSLLSPFFTPNAAPAEFIPLYEKVAKCLSEDNSDLVFMLLTKFDVQQWLSSTKPPLSDRTRLLESIHLALTAWGLEPEEDIMMPFNLFCKHWTHLLLYQFPDQYSDVLRLLVQSSAEQLLSPECWKATLKALGCYAPSIQQGEASVESSVLHSASDVLLSDKQVTETVQWLSDFFYKLRLSKLDFKSFGLFSKWSPYMADVKTFLGYLVKRLTDLELASLAQDPTASSKEVLRSLHSQIIQLFKPWILVLEDTESSHQRHYPWLESDTVVASSLVQLFTDCVSSLHASFKDKLLPGDEGALRLHLLHYTESCTAPRMPEFILYAFHSAYQKLEWKDLHPDQRLMEAFFKVERGSPKSCFLFLGSVLCRVNWVSVLSDAWSPSPLPETQSMVVCLLFMMVLLAKEAQLVDETDSPLLSLLGQTSSLSWHLVDFVSYQSVLGYFSSHYPPSVILAQDCSAELIVRLLKVSAGLSLPADSRKHVDIVPKCQAFTHQMAQFLSALEQDGKVAFPALGQEVSKLLDDIITFNPPDMDSQTRHMALSSLFMEVLMMMNSAAVPTAEYLGVSIRTWIGQKVHGLVVLPLLTAACQSLASVRHMAETTEACITAYFKESSLDQNLGWGPILVSLQVPELTMQEFLQECLALGSCLTLYVYLLQCLNSEQTVKNEMKVLLILSTWLEHVYPSSAQEEAKLLLWWHQALQLSLVQLEQDDSVLTESVIRILLMLQGRQSLMAEERLSSGILGAIGLGRKSPLSNRFRVVARSMAAFLSVQVPAEDQIRLKPSSELHLTPKAQQVLAALESMTLSKQYVEYQDQILHAVQFIRHPGHCLQNGKSFLAFFVNRLYPEVHYLDNIR",
                "length": 2510,
                "header": "tr|A0A8I6ACL1-1|A0A8I6ACL1_RAT Computationally mapped isoform of Ectopic P-granules autophagy protein 5 homolog  OS=Rattus norvegicus OX=10116 GN=Epg5 PE=1 SV=1 CANONICAL=A0A0G2JZ84-1"
            },
            "locus": {
                "chromosome": "18",
                "start_pos": 71499735,
                "end_pos": 71404083,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000108039.1",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000108039.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000090805.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000090805.1"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [
        {
            "id": "rno:364902",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:364902",
            "resource": "KEGG Pathway"
        }
    ],
    "orthologs": [
        {
            "uniprot_canonical_ac": "Q80TA9-1",
            "protein_name": "Ectopic P granules protein 5 homolog",
            "gene_name": "Epg5",
            "tax_id": 10090,
            "organism": "Mus musculus",
            "sequence": {
                "sequence": "MAEAVKPRRAKAKASRTKGKEKKKHEALQTCDAGPLPETCREQESPCPASELKGDDLKSSADPQLHSDVCGWNESEMFDIPLTSLTIGDEGPPVQDTEDLKERGEVTAGDGDDEMELKVDPGDNVIAKGEPCKNFPEVEDHTLIQCGPPESTLQPDFPCTQQAVEGSHAREHPTRKQDEAALGCSKVFQNVSLHSSYEAKEVSQPPRVKKLYPELPAEIAEVPALVAVKPLLRSERLYPELPSQPEVTPFTKEQLKLLEPGSWLENVASYVEEFDNIAHQDRHEFYELLLNYSRCRKQLLLAEAELLTLMSDCHSAKSRLWHFKDEQMAVQGICADQVKVYGHHHYQRVEMNENVLGELKKLFDAKSEHLHQTLTLHSYTSVLSRLQVESYIFTLLNSSAALRSLAVYQADQVPKLTESIPSDVCQLKECISVLFMFTRRVSEDAQFHEDILLWLQKLVSVLQRVGCPGDHFFLLNHVLRCPAGIRKWAVPFIQIKVLNNPSGVFHFMQSLALLMSPVKNRAEFMCHMKPSEWKPSSSGPASGNWTLVDEAGEEDEDPETSWILLNEDDLVTLLSQFPFQELFQHLLGFKAKGDYLPETTRPQEMMKIFAFANSLVELLAVGLDTFNRARYRQFVKRIGYLIRMTLGYVSDHWAQYVSHSTGAGLTPQPYSMEKLQVEFDELFLRAVLHVLKAKRLGIWLFMSEMPFGTLSVQMLWKLLYLMHQVESGDLQQLCASLQPAECKRRLQDPEHFASFEKCLSSINSSEEICLLTAFAQMARARRTNVDEDFIKIIVLEIYEVSYVTLSTRETFSKVGRELLGAIAAVHPEIISVLLDRVQETIDQVGMVSLYLFKELPLYLWRPSAPEIAVIRDWLLNNNLTAVKNKLACVILEGLNWGFTEQGTLHLDQALHTEVALLVLEAYQKYLAQKPYTGLISESMKQVSYLASIVRYGETPETSFNQWAWNLILRLKLHKNDFGRQNFPVIPFCSTVPDMTESSMFHPLLKAVKSGLPIGCYLALAVTAVGHSLEKFCAEGIPLLGVLVQSRHLRAVVHALDKILPVFYPYQCYLLKNEQFLSNLLLFLQLDSGVPQGVTQQVTHRVAQHLTGAVHGDNVKLLSSMIQAHICVSTQPDGVGPVAVLEFWVQALISQHLWYREQPILFLMDHLCKTAFHLMQEDCVQKLLYQQHKNALGYHCDRSLLSSLVNWIVAGNITPSFVEGLSTSTQVWFAWTVLNMESIFEEDSQLRRVVERELVINAFSPDQALKKAQVQLKLPIVPSLQRLLIYRWAHQALVTPSDHPLLPLIWQKFFLLYLHRPGPQYGLPVDGCIGRRFFQSPSHVNLLKDMKRRLTEVADFHYAASKALRVPAEGSEGTPEGQAGTPGFLTSPELHRELVRLFNVYVLWLEDENFQKGDTYIPSLPKHYDVHRLAKVMQNQQDLWMEYVNMERIQHEFQETVALWTQAKLESHAAPCSSSAQLDFTDPLLAKARVLSNLEKHEAPHPPLLLHPVRPPVPLIPSAALLTQKDSTQLMCTDLNLLQQQARSATLRESQQVALDGELLETMPKQYVNREDQATLHLECRGSSGKKCQGAAVVTVQFEGMNKNEAVSQQIHVLQKEVRQLQAEAAQPPALNVVEAAVHAENLITALVNTYKLQPTPGVQKLGISLFFTVVDHVSDETQRHPPTRQFFTSCIEILGQVFVSGTKSECRKLLQTILKNRRLCSLLAPFFTPNAAPAEFIQLYERVVTCLREDNSDVIFMLLTKFDIQQWLNSTKPPLSDRTRLLESIHLALTAWGLEPEEDILMPFNLFCKHWTHLLLYQFPDQYSDVLRLLVQSSAEQLLSPECWKATLRALGCYAPSSQQGAASVESSGLHSASRVLLSDKQVMETVQWLSDFFYKLRLSKLDFKSFGLFSKWSPYMADVKTFLGYLVKRLTDLEIASLSQDPTASSKEVLRSLHAQIIQLFKPWILVLEDAESSHQRHYPWLESDTAVASSIVQLFSDCVGSLHTSFKDRLLPGDEGALRLHLLHYCETCTAPKMPEFILYAFHSAYQRLEWKDLHPDQRLMEAFFKVERGSPKSCFLFLGSVLCRVNWVSVLSDAWNPSPLPETQSMAVCLLFMMVLLAKEAQLVDEPDSPLLSLLGQTSSLSWHLVDLVSYQSVLGYFSSHYPPSVVLANDCSSELIVKLLKVSAGLSAHADGRKHVDIVPKCQAFTHQMVQFLSALEQTGKITFPALEREISKLLDDIIIFNPPDMDSQTRHMALSSFFVEVLMMMNNAAVPTAEFLAVSIRTWIGQRVHGLIVLPLLTAACQSLASVRHMAEITEACIMAYFKESSLDQNLGWGPVLVSLQVPQLTARDFLEECLALGSCLTLYVYLLQCLNSEQTVKNDMKMLLVVSGWLEQVYPSSAQEEAKLFLWWHQILQLSLIQLEQNDSVLTESVIRILLMLQSRQSLMAEERLSSGILGAIGLGRRSPLSNRFRVAARSMAAFLLVQVPAEDQIRLKPSSELHLAPKAQQVLTALESMTLSKQYVEYQDQILHALQFIRHPGHCLQNGKSFLALLVNRLYPEVHYLDNIR",
                "length": 2572
            },
            "evidence": [
                {
                    "id": "45230871",
                    "url": "http://www.informatics.jax.org/homology/45230871",
                    "database": "MGI"
                }
            ],
            "common_name": "Mouse"
        },
        {
            "uniprot_canonical_ac": "Q9HCE0-1",
            "protein_name": "Ectopic P granules protein 5 homolog",
            "gene_name": "EPG5",
            "tax_id": 9606,
            "organism": "Homo sapiens",
            "sequence": {
                "sequence": "MAEAVKPQRRAKAKASRTKTKEKKKYETPQREESSEVSLPKTSREQEIPSLACEFKGDHLKVVTDSQLQDDASGQNESEMFDVPLTSLTISNEESLTCNTEPPKEGGEARPCVGDSAVTPKVHPGDNVGTKVETPKNFTEVEENMSVQGGLSESAPQSNFSYTQPAMENIQVRETQNSKEDKQGLVCSSEVPQNVGLQSSCPAKHGFQTPRVKKLYPQLPAEIAGEAPALVAVKPLLRSERLYPELPSQLELVPFTKEQLKILEPGSWLENVESYLEEFDSMAHQDRHEFYELLLNYSRCRKQLLLAEAELLTLTSDCQNAKSRLWQFKEEQMSVQGICADQVKVFSYHRYQRVEMNENALVELKKLFDAKSEHLHQTLALHSYTSVLSRLQVESYIYALLSSSAVLRSSAIHQQGRASKQTESIPSDLCQLKECISVLFMFTRRVNEDTQFHDDILLWLQKLVSVLQRVGCPGDHLFLLNHILRCPAGVSKWAVPFIQIKVLHNPSGVFHFMQSLALLMSPVKNRAEFMCHMKPSERKPSSSGPGSGTWTLVDEGGEEDEDPETSWILLNEDDLVTILAQFPFHELFQHLLGFKAKGDYLPETTRPQEMMKIFAFANSLVELLAVGLETFNRARYRQFVKRIGYMIRMTLGYVSDHWAQYVSHNQGSGLAQQPYSMEKLQVEFDELFLRAVLHVLKAKRLGIWLFMSEMPFGTLSVQMLWKLFYLMHQVESENLQQLSSSLQPAQCKQQLQDPEHFTNFEKCLSSMNSSEEICLLTTFAQMAQARRTNVDEDFIKIIVLEIYEVSYVTLSTRETFSKVGRELLGTITAVHPEIISVLLDRVQETIDQVGMVSLYLFKELPLYLWQPSASEIAVIRDWLLNYNLTVVKNKLACVILEGLNWGFAKQATLHLDQAVHAEVALMVLEAYQKYLAQKPYAGILSESMKQVSYLASIVRYGETPETSFNQWAWNLILRLKLHKNDYGIQPNCPAVPFSVTVPDMTESPTFHPLLKAVKAGMPIGCYLALSMTAVGHSIEKFCAEGIPLLGILVQSRHLRTVVHVLDKILPLFYPCQYYLLKNEQFLSHLLLFLHLDSGVPQGVTQQVTHKVAQHLTGASHGDNVKLLNSMIQAHISVSTQPNEVGPVAVLEFWVQALISQHLWYREQPILFLMDHLCKAAFQLMQEDCIQKLLYQQHKNALGYHCDRSLLSSLVSWIVAGNITPSFVEGLATPTQVWFAWTVLNMESIFEEDSQLRRVIEGELVINSAFTPDQALKKAQTQLKLPIVPSLQRLLIYRWAHQALVTPSDHPLLPLIWQKFFLLYLHRPGPQYGLPIDGCIGRRFFQSPAHINLLKEMKRRLTEVADFHHAASKALRVPAEGSEGLPESHSGTPGYLTSPELHKELVRLFNVYILWLEDENFQKGDTYIPSLPKHYDIHRLAKVMQNQQDLWMEYLNMERIYHEFQETVGLWTQAKLESHSTPCSLSVQLDFTDPLLAKERVLSNLRKHEAPQPPLALHPTKPPVPVISSAVLLSQKDATQLVCTDLNLLQQQARTAALRESQQVALDGELLDTMPKQYVNREEQTTLHLECRGSSGKKCQGAAVVTVQFEGMHKNEAISQQLHVLRKEVKQLQAEAAKPPSLNIVEAAVHAENLITALVNAYKLQPTPGIQKVGISLFFTIVDYVSDETQRHPPTRQFFTSCIEILGQVFISGIKSECRKVLETILKNSRLCSLLSPFFTPNAAPAEFIQLYEQVVKFLSEDNSDMIFMLLTKFDLKQWLSATKPPLSDRTRLLESIHLALTAWGLEPDEDILMPFNLFCKHWTYLLLYQFPDQYSDILRLLMQSSAEQLLSPECWKATLRALGCCAPSCQQGAASTEGAVLPSSSDALLSDKQVMETIQWLSDFFYKLRLSKMDFKSFGLFSKWSPYMADVKTFLGYLVKRLIDLEMTCLAQDPTASRKTVLKSLHSVIIQLFKPWILVLEDNESSQQRHYPWLESDTVVASSIVQLFTDCIDSLHESFKDKLLPGDAGALWLHLMHYCEACTAPKMPEFILYAFHSTYRKLPWKDLHPDQMLMEAFFKVERGSPKSCFLFLGSVLCEVNWVSVLSDAWNSSPHPETRSMIVCLLFMMILLAKEVQLVDQTDSPLLSLLGQTSSLSWHLVDIVSYQSVLSYFSSHYPPSIILAKESYAELIMKLLKVSAGLSIPTDSQKHLDAVPKCQAFTHQMVQFLSTLEQNGKITLAVLEQEMSKLLDDIIVFNPPDMDSQTRHMALSSLFMEVLMMMNNATIPTAEFLRGSIRTWIGQKMHGLVVLPLLTAACQSLASVRHMAETTEACITAYFKESPLNQNSGWGPILVSLQVPELTMEEFLQECLTLGSYLTLYVYLLQCLNSEQTLRNEMKVLLILSKWLEQVYPSSVEEEAKLFLWWHQVLQLSLIQTEQNDSVLTESVIRILLLVQSRQNLVAEERLSSGILGAIGFGRKSPLSNRFRVVARSMAAFLSVQVPMEDQIRLRPGSELHLTPKAQQALNALESMASSKQYVEYQDQILQATQFIRHPGHCLQDGKSFLALLVNCLYPEVHYLDHIR",
                "length": 2579
            },
            "evidence": [
                {
                    "id": "45230871",
                    "url": "http://www.informatics.jax.org/homology/45230871",
                    "database": "MGI"
                }
            ],
            "common_name": "Human"
        }
    ],
    "go_annotation": {
        "categories": [
            {
                "name": "Biological Process",
                "total": 7,
                "go_terms": [
                    {
                        "name": "autophagosome maturation",
                        "id": "GO:0097352",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097352",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JZ84",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JZ84"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "autophagy",
                        "id": "GO:0006914",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006914",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JZ84",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JZ84"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "endosome to lysosome transport",
                        "id": "GO:0008333",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008333",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JZ84",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JZ84"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "endocytic recycling",
                        "id": "GO:0032456",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032456",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JZ84",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JZ84"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "toll-like receptor 9 signaling pathway",
                        "id": "GO:0034162",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034162",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JZ84",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JZ84"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cellular response to dsDNA",
                        "id": "GO:1990786",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990786",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JZ84",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JZ84"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "nucleotide transport",
                        "id": "GO:0006862",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006862",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JZ84",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JZ84"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 3,
                "go_terms": [
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            "name": "homologset.mgi",
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