{
    "uniprot_canonical_ac": "A0A8I5ZLR9-1",
    "uniprot_ac": "A0A8I5ZLR9",
    "uniprot_id": "A0A8I5ZLR9_RAT",
    "mass": {
        "chemical_mass": 125329.0,
        "monoisotopic_mass": 125329.0
    },
    "refseq": {},
    "gene_names": [
        {
            "name": "Diaph2",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A8I5ZLR9",
            "id": "A0A8I5ZLR9"
        },
        {
            "name": "AABR07040412.1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A8I5ZLR9",
            "id": "A0A8I5ZLR9"
        }
    ],
    "protein_names": [
        {
            "name": "Diaphanous-related formin 2",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A8I5ZLR9"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0060690",
            "recommended_name": {
                "id": "DOID:0060690",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0060690",
                "name": "autosomal dominant auditory neuropathy 1",
                "description": "An autosomal dominant nonsyndromic deafness characterized by preservation of outer hair cell function and abnormal or absent auditory brainstem responses that has_material_basis_in heterozygous mutation in the DIAPH3 gene on chromosome 13q."
            },
            "synonyms": [
                {
                    "id": "DOID:0060690",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060690",
                    "name": "AUNA1",
                    "description": ""
                },
                {
                    "id": "DOID:0060690",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060690",
                    "name": "NSDAN",
                    "description": ""
                },
                {
                    "id": "DOID:0060690",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060690",
                    "name": "nonsyndromic dominant auditory neuropathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0012196",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012196",
                    "name": "autosomal dominant auditory neuropathy 1",
                    "description": "Any auditory neuropathy in which the cause of the disease is a mutation in the DIAPH3 gene."
                },
                {
                    "id": "MONDO:0012196",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012196",
                    "name": "AUNA1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012196",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012196",
                    "name": "DIAPH3 auditory neuropathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0012196",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012196",
                    "name": "NSDAN",
                    "description": ""
                },
                {
                    "id": "MONDO:0012196",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012196",
                    "name": "auditory neuropathy caused by mutation in DIAPH3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012196",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012196",
                    "name": "auditory neuropathy, autosomal dominant, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012196",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012196",
                    "name": "autosomal dominant auditory neuropathy type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012196",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012196",
                    "name": "nonsyndromic dominant auditory neuropathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0012196",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012196",
                    "name": "auditory neuropathy, autosomal dominant, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012196",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012196",
                    "name": "auditory neuropathy, nonsyndromic dominant",
                    "description": ""
                },
                {
                    "id": "MIM:609129",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/609129",
                    "name": "Auditory neuropathy, autosomal dominant 1",
                    "description": "Auditory neuropathy, autosomal dominant 1"
                }
            ],
            "evidence": [
                {
                    "id": "0060690",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0060690"
                }
            ]
        },
        {
            "disease_id": "DOID:0080858",
            "recommended_name": {
                "id": "DOID:0080858",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0080858",
                "name": "primary ovarian insufficiency 2A",
                "description": "A primary ovarian insufficiency that has_material_basis_in mutation in the DIAPH2 gene on chromosome Xq22."
            },
            "synonyms": [
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "premature ovarian failure 2A",
                    "description": "Any primary ovarian failure in which the cause of the disease is a mutation in the DIAPH2 gene."
                },
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "DIAPH2 primary ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "premature ovarian failure 2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "premature ovarian failure 2A, X-linked dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "premature ovarian failure type 2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "primary ovarian failure caused by mutation in DIAPH2",
                    "description": ""
                },
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "POF2A",
                    "description": ""
                },
                {
                    "id": "MIM:300511",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/300511",
                    "name": "Premature ovarian failure 2A",
                    "description": "Premature ovarian failure 2A"
                }
            ],
            "evidence": [
                {
                    "id": "0080858",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0080858"
                }
            ]
        },
        {
            "disease_id": "DOID:5426",
            "recommended_name": {
                "id": "DOID:5426",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:5426",
                "name": "primary ovarian insufficiency",
                "description": "An ovarian disease where ovaries do not produce estrogen despite high levels of circulating gonadotropins in women under 40."
            },
            "synonyms": [
                {
                    "id": "DOID:5426",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:5426",
                    "name": "premature ovarian failure",
                    "description": ""
                },
                {
                    "id": "DOID:5426",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:5426",
                    "name": "hypergonadotropic hypogonadism",
                    "description": ""
                },
                {
                    "id": "DOID:5426",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:5426",
                    "name": "premature menopause",
                    "description": ""
                },
                {
                    "id": "DOID:5426",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:5426",
                    "name": "premature ovarian insufficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "premature ovarian failure 1",
                    "description": "Any primary ovarian failure in which the cause of the disease is a mutation in the FMR1 gene."
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "ovarian failure, premature",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "FMR1 primary ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "fragile x-associated primary ovarian insufficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "premature ovarian failure 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "premature ovarian failure type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "primary ovarian failure caused by mutation in FMR1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "FMR1-related premature ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "FMR1-related primary ovarian insufficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "Pof1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "familial premature ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "fragile X-associated primary ovarian insufficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "hypergonadotropic ovarian failure, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "idiopathic familial premature ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "premature ovarian failure, X-linked",
                    "description": ""
                },
                {
                    "id": "MIM:311360",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/311360",
                    "name": "Premature ovarian failure 1",
                    "description": "Premature ovarian failure 1"
                }
            ],
            "evidence": [
                {
                    "id": "5426",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:5426"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Rattus norvegicus",
            "taxid": 10116,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A8I5ZLR9",
                    "url": "https://www.uniprot.org/uniprot/A0A8I5ZLR9"
                }
            ],
            "common_name": "Rat"
        }
    ],
    "gene": [
        {
            "name": "Diaph2",
            "url": "https://www.uniprot.org/uniprot/A0A8I5ZLR9",
            "locus": {}
        }
    ],
    "crossref": [
        {
            "id": "ENSRNOG00000057826",
            "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000057826",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "IPR010472",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR010472",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR010473",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR010473",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR011989",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR011989",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR014767",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR014767",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR014768",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR014768",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR015425",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR015425",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR016024",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR016024",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR042201",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR042201",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR044933",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR044933",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "ANHDNRR",
            "url": "https://omabrowser.org/oma/group/ANHDNRR/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR45691",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR45691",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR45691:SF3",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR45691:SF3",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF02181",
            "url": "http://pfam.xfam.org/family/PF02181",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF06367",
            "url": "http://pfam.xfam.org/family/PF06367",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF06371",
            "url": "http://pfam.xfam.org/family/PF06371",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "15011308",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=15011308",
            "database": "RGD",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "1564399",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1564399",
            "database": "RGD",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "A0A0G2JTM1",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JTM1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0G2JTM1-1",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JTM1-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I5ZLR9",
            "url": "https://www.uniprot.org/uniprot/A0A8I5ZLR9",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I5ZLR9-1",
            "url": "https://www.uniprot.org/uniprot/A0A8I5ZLR9-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I5ZUN2",
            "url": "https://www.uniprot.org/uniprot/A0A8I5ZUN2",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I5ZUN2-1",
            "url": "https://www.uniprot.org/uniprot/A0A8I5ZUN2-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I6AK57",
            "url": "https://www.uniprot.org/uniprot/A0A8I6AK57",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I6AK57-1",
            "url": "https://www.uniprot.org/uniprot/A0A8I6AK57-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MEQPGAAASGAGGGGGGEEPGVGRSNKRGTGNRAANEEETKNKPKLNIQIKTLADDVRDRITSFRKSAIKKEKPLIQHPTDSQAAMGEVPSAQILHDERSLILSEKEVLDLFEKMMEDMNLNEEKKAPLRDKDFTTKREMVVQYISATAKSIVGSKVMGGLKNNKHEFTLSSQEYVHELRSGISDEKLLNCLESLRVSLTSNPVSWVNNFGYEGLGVLLDVLEKLLDKKQQENIDKKNQYKIIQCLKAFMNNKFGLQRILGDERSLLLLARAIDPKQQNMMTEIVKILSAICIVGEENILDKLLGGITAAAERNNRERFSPIVEGLENNEALHLQVACMQFINALVTSPYDLDFRIHLRNEFLRCGLKAMLPSLKEKENDELDIQLRVFEENKEDDLTELSHRLNDIRAEMDDMNEVFHLLYNMLKDTAAEGYLLSILQHFLLIRNDYYIRPQYYKIIEECVSQIVLHCSGMDPDFKYRQRIDFDFTHLIDACVNKAKVEESEQKAMEFSKKFDEEFTARQEAQAEIQKRDEKIKELESEIQQLQAQGPGSAFPGPPPPPPLPGAGPCPPPPPPPPPLPGVGPPPPPPLPGTAPPPPPLFGAPLLPPPPGGITPSLPGPVELPYGMKQKKLYNPEVSMKRINWSKIEPRDLSENCVWLKLKEEKYENPDLFAKLALTFPSQMKGQRHGETSEENRIGPQKKKMKELRILDTKTAQNLSIFLGSYRMPYEEIKNIILEVNEELLSEALIQNLVKYLPEQNVLRELAQLKNEYDDLCEPEQFGVVMSTVNMLRPRLTSILFKLTFEEHVNNIKPSIIAVTLACEELKKSESFNRLLELILLVGNYMNSGSRNAQSLGFKINFLCKIKDTKSADQKTTLLHFLAEICDEQHRDILKFPEELEHVESASKVSAQILKSNLVAMEQSILHLESNIKNFPKAESLHDKFVEKMMSFTQNAREQYDKLSTMHSNMLKLYESLGEYFIFDPNIVTIEEFFGDLNTFRTLFLEALKENHKRKEMEEKSRRAKLAKEKAEQEKLERQKKKKQLIDINKEGDETGVMDNLLEALQSGAAFRDRRKRIPRNPDNRRPTLERSRSRHNGAMPSK",
        "length": 1101,
        "header": "tr|A0A8I5ZLR9-1|A0A8I5ZLR9_RAT Isoform 1 of Diaphanous-related formin 2  OS=Rattus norvegicus OX=10116 GN=Diaph2 PE=1 SV=1 CANONICAL=A0A8I5ZLR9-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A0G2JTM1-1",
            "url": "",
            "sequence": {
                "sequence": "MEQPGAAASGAGGGGGGEEPGVGRSNKRGTGNRAANEEETKNKPKLRDRITSFRKSAIKKEKPLIQHPTDSQAAMGEVPSAQILHDERSLILSEKEVLDLFEKMMEDMNLNEEKKAPLRDKDFTTKREMVVQYISATAKSIVGSKVMGGLKNNKHEFTLSSQEYVHELRSGISDEKLLNCLESLRVSLTSNPVSWVNNFGYEGLGVLLDVLEKLLDKKQQENIDKKNQYKIIQCLKAFMNNKFGLQRILGDERSLLLLARAIDPKQQNMMTEIVKILSAICIVGEENILDKLLGGITAAAERNNRERFSPIVEGLENNEALHLQVACMQFINALVTSPYDLDFRIHLRNEFLRCGLKAMLPSLKEKENDELDIQLRVFEENKEDDLTELSHRLNDIRAEMDDMNEVFHLLYNMLKDTAAEGYLLSILQHFLLIRNDYYIRPQYYKIIEECVSQIVLHCSGMDPDFKYRQRIDFDFTHLIDACVNKAKVEESEQKAMEFSKKFDEEFTARQEAQAEIQKRDEKIKELESEIQQLQAQGPGSAFPGPPPPPPLPGAGPCPPPPPPPPPLPGVGPPPPPPLPGTAPPPPPLFGAPLLPPPPGGITPSLPGPVELPYGMKQKKLYNPEVSMKRINWSKIEPRDLSENCVWLKLKEEKYENPDLFAKLALTFPSQMKGQRHGETSEENRIGPQKKKMKELRILDTKTAQNLSIFLGSYRMPYEEIKNIILEVNEELLSEALIQNLVKYLPEQNVLRELAQLKNEYDDLCEPEQFGVVMSTVNMLRPRLTSILFKLTFEEHVNNIKPSIIAVTLACEELKKSESFNRLLELILLVGNYMNSGSRNAQSLGFKINFLCKIKDTKSADQKTTLLHFLAEICDEQHRDILKFPEELEHVESASKVSAQILKSNLVAMEQSILHLESNIKNFPKAESLHDKFVEKMMSFTQNAREQYDKLSTMHSNMLKLYESLGEYFIFDPNIVTIEEFFGDLNTFRTLFLEKPHLESRKKDNSG",
                "length": 1006,
                "header": "tr|A0A0G2JTM1-1|A0A0G2JTM1_RAT Computationally mapped isoform of Diaphanous-related formin 2  OS=Rattus norvegicus OX=10116 GN=Diaph2 PE=1 SV=2 CANONICAL=A0A8I5ZLR9-1"
            },
            "locus": {
                "chromosome": "X",
                "start_pos": 93006819,
                "end_pos": 92395597,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000082451.2",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000082451.2"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000068765.2",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000068765.2"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8I5ZLR9-1",
            "url": "",
            "sequence": {
                "sequence": "MEQPGAAASGAGGGGGGEEPGVGRSNKRGTGNRAANEEETKNKPKLNIQIKTLADDVRDRITSFRKSAIKKEKPLIQHPTDSQAAMGEVPSAQILHDERSLILSEKEVLDLFEKMMEDMNLNEEKKAPLRDKDFTTKREMVVQYISATAKSIVGSKVMGGLKNNKHEFTLSSQEYVHELRSGISDEKLLNCLESLRVSLTSNPVSWVNNFGYEGLGVLLDVLEKLLDKKQQENIDKKNQYKIIQCLKAFMNNKFGLQRILGDERSLLLLARAIDPKQQNMMTEIVKILSAICIVGEENILDKLLGGITAAAERNNRERFSPIVEGLENNEALHLQVACMQFINALVTSPYDLDFRIHLRNEFLRCGLKAMLPSLKEKENDELDIQLRVFEENKEDDLTELSHRLNDIRAEMDDMNEVFHLLYNMLKDTAAEGYLLSILQHFLLIRNDYYIRPQYYKIIEECVSQIVLHCSGMDPDFKYRQRIDFDFTHLIDACVNKAKVEESEQKAMEFSKKFDEEFTARQEAQAEIQKRDEKIKELESEIQQLQAQGPGSAFPGPPPPPPLPGAGPCPPPPPPPPPLPGVGPPPPPPLPGTAPPPPPLFGAPLLPPPPGGITPSLPGPVELPYGMKQKKLYNPEVSMKRINWSKIEPRDLSENCVWLKLKEEKYENPDLFAKLALTFPSQMKGQRHGETSEENRIGPQKKKMKELRILDTKTAQNLSIFLGSYRMPYEEIKNIILEVNEELLSEALIQNLVKYLPEQNVLRELAQLKNEYDDLCEPEQFGVVMSTVNMLRPRLTSILFKLTFEEHVNNIKPSIIAVTLACEELKKSESFNRLLELILLVGNYMNSGSRNAQSLGFKINFLCKIKDTKSADQKTTLLHFLAEICDEQHRDILKFPEELEHVESASKVSAQILKSNLVAMEQSILHLESNIKNFPKAESLHDKFVEKMMSFTQNAREQYDKLSTMHSNMLKLYESLGEYFIFDPNIVTIEEFFGDLNTFRTLFLEALKENHKRKEMEEKSRRAKLAKEKAEQEKLERQKKKKQLIDINKEGDETGVMDNLLEALQSGAAFRDRRKRIPRNPDNRRPTLERSRSRHNGAMPSK",
                "length": 1101,
                "header": "tr|A0A8I5ZLR9-1|A0A8I5ZLR9_RAT Isoform 1 of Diaphanous-related formin 2  OS=Rattus norvegicus OX=10116 GN=Diaph2 PE=1 SV=1 CANONICAL=A0A8I5ZLR9-1"
            },
            "locus": {
                "chromosome": "X",
                "start_pos": 93229761,
                "end_pos": 92395597,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000095712.1",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000095712.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000078839.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000078839.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8I5ZUN2-1",
            "url": "",
            "sequence": {
                "sequence": "MEQPGAAASGAGGGGGGEEPGVGRSNKRGTGNRAANEEETKNKPKLRDRITSFRKSAIKKEKPLIQHPTDSQAAMGEVPSAQILHDERSLILSEKEVLDLFEKMMEDMNLNEEKKAPLRDKDFTTKREMVVQYISATAKSIVGSKVMGGLKNNKHEFTLSSQEYVHELRSGISDEKLLNCLESLRVSLTSNPVSWVNNFGYEGLGVLLDVLEKLLDKKQQENIDKKNQYKIIQCLKAFMNNKFGLQRILGDERSLLLLARAIDPKQQNMMTEIVKILSAICIVGEENILDKLLGGITAAAERNNRERFSPIVEGLENNEALHLQVACMQFINALVTSPYDLDFRIHLRNEFLRCGLKAMLPSLKEKENDELDIQLRVFEENKEDDLTELSHRLNDIRAEMDDMNEVFHLLYNMLKDTAAEGYLLSILQHFLLIRNDYYIRPQYYKIIEECVSQIVLHCSGMDPDFKYRQRIDFDFTHLIDACVNKAKVEESEQKAMEFSKKFDEEFTARQEAQAEIQKRDEKIKELESEIQQLQAQGPGSAFPGPPPPPPLPGAGPCPPPPPPPPPLPGVGPPPPPPLPGTAPPPPPLFGAPLLPPPPGGITPSLPGPVELPYGMKQKKLYNPEVSMKRINWSKIEPRDLSENCVWLKLKEEKYENPDLFAKLALTFPSQMKGQRHGETSEENRIGPQKKKMKELRILDTKTAQNLSIFLGSYRMPYEEIKNIILEVNEELLSEALIQNLVKYLPEQNVLRELAQLKNEYDDLCEPEQFGVVMSTVNMLRPRLTSILFKLTFEEHVNNIKPSIIAVTLACEELKKSESFNRLLELILLVGNYMNSGSRNAQSLGFKINFLCKIKDTKSADQKTTLLHFLAEICDEQHRDILKFPEELEHVESASKVSAQILKSNLVAMEQSILHLESNIKNFPKAESLHDKFVEKMMSFTQNAREQYDKLSTMHSNMLKLYESLGEYFIFDPNIVTIEEFFGDLNTFRTLFLEALKENHKRKEMEEKSRRAKLAKEKAEQEKLERQKKKKQLIDINKEGDETGVMDNLLEALQSGAAFRDRRKRIPRNPDNRRPTLERSRSRHNGAMPSK",
                "length": 1090,
                "header": "tr|A0A8I5ZUN2-1|A0A8I5ZUN2_RAT Computationally mapped isoform of Diaphanous-related formin 2  OS=Rattus norvegicus OX=10116 GN=Diaph2 PE=1 SV=1 CANONICAL=A0A8I5ZLR9-1"
            },
            "locus": {
                "chromosome": "X",
                "start_pos": 93229761,
                "end_pos": 92395597,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000115579.1",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000115579.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000082731.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000082731.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8I6AK57-1",
            "url": "",
            "sequence": {
                "sequence": "MEQPGAAASGAGGGGGGEEPGVGRSNKRGTGNRAANEEETKNKPKLRDRITSFRKSAIKKEKPLIQHPTDSQAAMGEVPSAQILHDERSLILSEKEVLDLFEKMMEDMNLNEEKKAPLRDKDFTTKREMVVQYISATAKSGGLKNNKHEFTLSSQEYVHELRSGISDEKLLNCLESLRVSLTSNPVSWVNNFGYEGLGVLLDVLEKLLDKKQQENIDKKNQYKIIQCLKAFMNNKFGLQRILGDERSLLLLARAIDPKQQNMMTEIVKILSAICIVGEENILDKLLGGITAAAERNNRERFSPIVEGLENNEALHLQVACMQFINALVTSPYDLDFRIHLRNEFLRCGLKAMLPSLKEKENDELDIQLRVFEENKEDDLTELSHRLNDIRAEMDDMNEVFHLLYNMLKDTAAEGYLLSILQHFLLIRNDYYIRPQYYKIIEECVSQIVLHCSGMDPDFKYRQRIDFDFTHLIDACVNKAKVEESEQKAMEFSKKFDEEFTARQEAQAEIQKRDEKIKELESEIQQLQAQGPGSAFPGPPPPPPLPGAGPCPPPPPPPPPLPGVGPPPPPPLPGTAPPPPPLFGAPLLPPPPGGITPSLPGPVELPYGMKQKKLYNPEVSMKRINWSKIEPRDLSENCVWLKLKEEKYENPDLFAKLALTFPSQMKGQRHGETSEENRIGPQKKKMKELRILDTKTAQNLSIFLGSYRMPYEEIKNIILEVNEELLSEALIQNLVKYLPEQNVLRELAQLKNEYDDLCEPEQFGVVMSTVNMLRPRLTSILFKLTFEEHVNNIKPSIIAVTLACEELKKSESFNRLLELILLVGNYMNSGSRNAQSLGFKINFLCKIKDTKSADQKTTLLHFLAEICDEQHRDILKFPEELEHVESASKVSAQILKSNLVAMEQSILHLESNIKNFPKAESLHDKFVEKMMSFTQNAREQYDKLSTMHSNMLKLYESLGEYFIFDPNIVTIEEFFGDLNTFRTLFLEALKENHKRKEMEEKSRRAKLAKEKAEQEKLERQKKKKQLIDINKEGDETGVMDNLLEALQSGAAFRDRRKRIPRNPDNRRPTLERSRSRHNGAMPSK",
                "length": 1083,
                "header": "tr|A0A8I6AK57-1|A0A8I5ZLR9_RAT Computationally mapped isoform of Diaphanous-related formin 2  OS=Rattus norvegicus OX=10116 GN=Diaph2 PE=1 SV=1 CANONICAL=A0A8I5ZLR9-1"
            },
            "locus": {
                "chromosome": "X",
                "start_pos": 93229761,
                "end_pos": 92395597,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000105363.1",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000105363.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000093476.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000093476.1"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [],
    "orthologs": [],
    "go_annotation": {
        "categories": [
            {
                "name": "Molecular Function",
                "total": 2,
                "go_terms": [
                    {
                        "name": "actin binding",
                        "id": "GO:0003779",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003779",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A8I5ZLR9",
                                "url": "https://www.uniprot.org/uniprot/A0A8I5ZLR9"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "small GTPase binding",
                        "id": "GO:0031267",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031267",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A8I5ZLR9",
                                "url": "https://www.uniprot.org/uniprot/A0A8I5ZLR9"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Biological Process",
                "total": 1,
                "go_terms": [
                    {
                        "name": "actin filament polymerization",
                        "id": "GO:0030041",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030041",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A8I5ZLR9",
                                "url": "https://www.uniprot.org/uniprot/A0A8I5ZLR9"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [
        {
            "start_pos": 642,
            "end_pos": 644,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 716,
            "end_pos": 718,
            "annotation": "n_glycosylation_sequon"
        }
    ],
    "ptm_annotation": [],
    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
        }
    ],
    "section_stats": [
        {
            "table_id": "glycosylation",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported_with_glycan",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_predicted",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_automatic_literature_mining",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "phosphorylation",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "snv",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "snv_disease",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "snv_non_disease",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "publication",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                }
            ],
            "sort_fields": []
        }
    ]
}