{
    "uniprot_canonical_ac": "Q5BK30-1",
    "uniprot_ac": "Q5BK30",
    "uniprot_id": "DAW1_RAT",
    "mass": {
        "chemical_mass": 45859.0,
        "monoisotopic_mass": 45859.0
    },
    "refseq": {
        "ac": "NP_001020196",
        "name": "dynein assembly factor with WD repeat domains 1",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001020196"
    },
    "gene_names": [
        {
            "name": "Daw1",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/Q5BK30",
            "id": "Q5BK30"
        },
        {
            "name": "Daw1",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001020196",
            "id": "NP_001020196"
        },
        {
            "name": "Wdr69",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001020196",
            "id": "NP_001020196"
        },
        {
            "name": "Wdr69",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q5BK30",
            "id": "Q5BK30"
        }
    ],
    "protein_names": [
        {
            "name": "Dynein assembly factor with WD repeat domains 1",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "Q5BK30"
        },
        {
            "name": "Outer row dynein assembly protein 16 homolog",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q5BK30"
        },
        {
            "name": "WD repeat-containing protein 69; outer row dynein assembly protein 16 homolog; dynein assembly factor with WDR repeat domains 1",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001020196",
            "id": "NP_001020196"
        },
        {
            "name": "WD repeat-containing protein 69",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q5BK30"
        },
        {
            "name": "dynein assembly factor with WD repeat domains 1",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001020196",
            "id": "NP_001020196"
        }
    ],
    "function": [
        {
            "annotation": "Required for axonemal dynein assembly and ciliary motility in ciliated organs, including Kupffer's vesicle, during embryogenesis. Facilitates the onset of robust cilia motility during development.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q5BK30",
                    "url": "https://www.uniprot.org/uniprot/Q5BK30#function"
                },
                {
                    "database": "UniProtKB",
                    "id": "Q8N136",
                    "url": "https://www.uniprot.org/uniprot/Q8N136#function"
                }
            ]
        }
    ],
    "disease": [
        {
            "disease_id": "DOID:0050144",
            "recommended_name": {
                "id": "DOID:0050144",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0050144",
                "name": "Kartagener syndrome",
                "description": "A primary ciliary dyskinesia that is characterized by sinusitis, bronchiectasis and situs inversus with dextrocardia resulting from dysfunction of the cilia during embryologic development."
            },
            "synonyms": [
                {
                    "id": "DOID:0050144",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0050144",
                    "name": "Kartagener's syndrome",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "0050144",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050144"
                }
            ]
        },
        {
            "disease_id": "DOID:0050545",
            "recommended_name": {
                "id": "DOID:0050545",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0050545",
                "name": "visceral heterotaxy",
                "description": "A physical disorder characterized by the abnormal distribution of the major visceral organs within the chest and abdomen."
            },
            "synonyms": [
                {
                    "id": "DOID:0050545",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0050545",
                    "name": "heterotaxia",
                    "description": ""
                },
                {
                    "id": "DOID:0050545",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0050545",
                    "name": "situs ambiguus",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "heterotaxy, visceral, 2, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "DTGA2",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "heterotaxy, visceral, 2, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "transposition of the great arteries, dextro-looped 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "HTX2",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "Htx",
                    "description": ""
                },
                {
                    "id": "MONDO:0011659",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011659",
                    "name": "heterotaxy, visceral, 3, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0011659",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011659",
                    "name": "HTX3",
                    "description": ""
                },
                {
                    "id": "MONDO:0011659",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011659",
                    "name": "heterotaxy, visceral, 3, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "heterotaxy, visceral, 1, X-linked",
                    "description": "X-linked visceral heterotaxy type 1 is a very rare form of heterotaxy that has only been reported in a few families. Heterotaxy is the right/left transposition of thoracic and/or abdominal organs. This condition is caused by mutations in the ZIC3 gene, is inherited in an X-linked recessive fashion, and is usually seen in males. Physical features include heart abnormalities such as dextrocardia, transposition of great vessels, ventricular septal defect, patent ductus arteriosus, pulmonic stenosis ; situs inversus, and missing (asplenia) and/or extra spleens (polysplenia).Affected individualscan also experience abnormalities in the development of the midline of the body, which can cause holoprosencephaly, myelomeningocele, urological anomalies, widely spaced eyes (hypertelorism), cleft palate, and abnormalities of the sacral spine and anus. Heterotaxia with recurrent respiratory infections are called primary ciliary dyskinesia."
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "ZIC3 visceral heterotaxy",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "congenital heart defects, nonsyndromic, 1, X-linked, X-linked recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "heterotaxy, visceral, 1, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "heterotaxy, visceral, 1, X-linked, X-linked recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "visceral heterotaxy caused by mutation in ZIC3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "HTX1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "X-linked visceral heterotaxy 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "congenital heart defects, multiple types, 1, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "dextrocardia with Other Cardiac malformations",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "heterotaxy, visceral, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "laterality, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "situs inversus, Complex Cardiac defects, and splenic defects, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0013887",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013887",
                    "name": "heterotaxy, visceral, 6, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0013887",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013887",
                    "name": "heterotaxy, visceral, 6, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0013887",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013887",
                    "name": "heterotaxy, visceral, 6, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0013887",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013887",
                    "name": "HTX6",
                    "description": ""
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "heterotaxy, visceral, 4, autosomal",
                    "description": "Any visceral heterotaxy in which the cause of the disease is a mutation in the ACVR2B gene."
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "ACVR2B visceral heterotaxy",
                    "description": ""
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "heterotaxy, visceral, 4, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "visceral heterotaxy caused by mutation in ACVR2B",
                    "description": ""
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "HTX4",
                    "description": ""
                },
                {
                    "id": "MIM:605376",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/605376",
                    "name": "Heterotaxy, visceral, 2, autosomal",
                    "description": "Heterotaxy, visceral, 2, autosomal"
                },
                {
                    "id": "MIM:306955",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/306955",
                    "name": "Heterotaxy, visceral, 1, X-linked",
                    "description": "Heterotaxy, visceral, 1, X-linked"
                },
                {
                    "id": "MIM:614779",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/614779",
                    "name": "Heterotaxy, visceral, 6, autosomal",
                    "description": "Heterotaxy, visceral, 6, autosomal"
                },
                {
                    "id": "MIM:613751",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/613751",
                    "name": "Heterotaxy, visceral, 4, autosomal",
                    "description": "Heterotaxy, visceral, 4, autosomal"
                }
            ],
            "evidence": [
                {
                    "id": "0050545",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050545"
                }
            ]
        },
        {
            "disease_id": "DOID:9562",
            "recommended_name": {
                "id": "DOID:9562",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:9562",
                "name": "primary ciliary dyskinesia",
                "description": "A ciliopathy that is characterized by impaired function of the cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube, middle ear) and fallopian tube."
            },
            "synonyms": [
                {
                    "id": "DOID:9562",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9562",
                    "name": "ciliary motility disorder",
                    "description": ""
                },
                {
                    "id": "DOID:9562",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9562",
                    "name": "immotile ciliary syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "primary ciliary dyskinesia 1",
                    "description": "Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the DNAI1 gene."
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "CILD1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "DNAI1 primary ciliary dyskinesia",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "ciliary dyskinesia, primary, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "primary ciliary dyskinesia 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "primary ciliary dyskinesia 1 with or without situs inversus",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "primary ciliary dyskinesia caused by mutation in DNAI1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "primary ciliary dyskinesia type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "Kartagener syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "PCD",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "Polynesian bronchiectasis",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "Siewert syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "ciliary dyskinesia, primary, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "ciliary dyskinesia, primary, 1, with or without situs inversus",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "dextrocardia, bronchiectasis, and sinusitis",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "immotile cilia syndrome",
                    "description": ""
                },
                {
                    "id": "MIM:244400",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/244400",
                    "name": "Kartagener syndrome",
                    "description": "Kartagener syndrome"
                }
            ],
            "evidence": [
                {
                    "id": "9562",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:9562"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Rattus norvegicus",
            "taxid": 10116,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q5BK30",
                    "url": "https://www.uniprot.org/uniprot/Q5BK30"
                }
            ],
            "common_name": "Rat"
        }
    ],
    "gene": [
        {
            "name": "Daw1",
            "url": "https://www.uniprot.org/uniprot/Q5BK30",
            "locus": {
                "chromosome": "9",
                "start_pos": 84472635,
                "end_pos": 84435552,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "ENSRNOG00000016247",
                        "url": "https://www.ensembl.org/id/ENSRNOG00000016247"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "ENSRNOG00000016247",
            "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000016247",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "cd00200",
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd00200",
            "database": "CDD",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "363267",
            "url": "https://www.ncbi.nlm.nih.gov/gene/363267",
            "database": "GeneID",
            "categories": [
                "Genome Annotation"
            ]
        },
        {
            "id": "IPR001680",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR001680",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR011047",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR011047",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR015943",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR015943",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR019775",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR019775",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR020472",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR020472",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR036322",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR036322",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "rno:363267",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:363267",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "TGQCSQV",
            "url": "https://omabrowser.org/oma/group/TGQCSQV/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "989707at2759",
            "url": "http://www.orthodb.org/?query=989707at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR19879",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR19879",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR19879:SF9",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR19879:SF9",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR22847",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR22847",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR22847:SF637",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR22847:SF637",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF00400",
            "url": "http://pfam.xfam.org/family/PF00400",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PR_Q5BK30",
            "url": "http://purl.obolibrary.org/obo/PR_Q5BK30",
            "database": "PRO",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "NP_001020196",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001020196",
            "database": "RefSeq",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "1561436",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1561436",
            "database": "RGD",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "A0A8I5ZTR7",
            "url": "https://www.uniprot.org/uniprot/A0A8I5ZTR7",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I5ZTR7-1",
            "url": "https://www.uniprot.org/uniprot/A0A8I5ZTR7-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I6ALT3",
            "url": "https://www.uniprot.org/uniprot/A0A8I6ALT3",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I6ALT3-1",
            "url": "https://www.uniprot.org/uniprot/A0A8I6ALT3-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8L2QSV3",
            "url": "https://www.uniprot.org/uniprot/A0A8L2QSV3",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8L2QSV3-1",
            "url": "https://www.uniprot.org/uniprot/A0A8L2QSV3-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q5BK30",
            "url": "https://www.uniprot.org/uniprot/Q5BK30",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q5BK30-1",
            "url": "https://www.uniprot.org/uniprot/Q5BK30-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MKLKSLLLRYYPPGIMLEYEKGGELKTKSIDLLELSPSTDVNTLVGEIQKVEPLITASRTKQVRLLVQRLQEKLRQHCDHNFYLFKVLRAHILPLTNVALNKAGSCFITGSYDRTCKVWDTASGEELHTLEGHRNVVYAIAFNNPYGDKIATGSFDKTCKLWSAETGKCYHTFRGHTAEIVCLSFNPQSTVVATGSMDTTAKLWDIQSGEEVVTLTGHLAEIISLSFDTSGDRIITGSFDHTVVVWDASTGRKVHTLIGHCAEISSALFSWDCSLILTGSMDKTCMLWDATSGKCVATLTGHDDEILDSCFDYTGKLIATASADGTARVYNATTRKCITKLEGHEGEISKISFNPQGNRLLTGSSDKTARIWDVQTGQCLQVLEGHTDEIFSCAFNYKGNIVITGSKDNSCRIWR",
        "length": 415,
        "header": "sp|Q5BK30-1|DAW1_RAT Isoform 1 of Dynein assembly factor with WD repeat domains 1  OS=Rattus norvegicus OX=10116 GN=Daw1 PE=2 SV=1 CANONICAL=Q5BK30-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A8I5ZTR7-1",
            "url": "",
            "sequence": {
                "sequence": "GKEKSLLRIMLEYEKGGELKTKSIDLLELSPSTDVNTLVGEIQKVEPLITASRTKQVRLLVQRLQEKLRQHCDHNFYLFKVLRAHILPLTNVALNKAGSCFITGSYDRTCKVWDTASGEELHTLEGHRNVVYAIAFNNPYGDKIATGSFDKTCKLWSAETGKCYHTFRGHTAEIVCLSFNPQSTVVATGSMDTTAKLWDIQSGEEVVTLTGHLAEIISLSFDTSGDRIITGSFDHTVVVWDASTGRKVHTLIGHCAEISSALFSWDCSLILTGSMDKTCMLWDATSGKCVATLTGHDDEILDSCFDYTGKLIATASADGTARVYNATTRKCITKLEGHEGEISKISFNPQGNRLLTGSSDKTARIWDVQTGQCLQVLEGHTDEIFSCAFNYKGNIVITGSKDNSCRIWR",
                "length": 409,
                "header": "tr|A0A8I5ZTR7-1|A0A8I5ZTR7_RAT Computationally mapped isoform of Dynein assembly factor with WD repeats 1  OS=Rattus norvegicus OX=10116 GN=Daw1 PE=4 SV=1 CANONICAL=Q5BK30-1"
            },
            "locus": {
                "chromosome": "9",
                "start_pos": 84472241,
                "end_pos": 84446639,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000107337.1",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000107337.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000081573.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000081573.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8I6ALT3-1",
            "url": "",
            "sequence": {
                "sequence": "MKLKSLLLRYYPPGIMLEYEKGGELKTKSIDLLELSPSTDVNTLVGEIQKVEPLITASRTKQVRLLVQRLQEKLRQHCDHNFYLFKVLRAHILPLTNVALNKAGSCFITGSYDRTCKVWDTASGEELHTLEGHRNVVYAIAFNNPYGKVHTLIGHCAEISSALFSWDCSLILTGSMDKTCMLWDATSGKCVATLTGHDDEILDSCFDYTGKLIATASADGTARVYNATTRKCITKLEGHEGEISKISFNPQGNRLLTGSSDKTARIWDVQTGQCLQVLEGHTDEIFSCAFNYKGNIVITGSKDNSCRIWR",
                "length": 310,
                "header": "tr|A0A8I6ALT3-1|A0A8I6ALT3_RAT Computationally mapped isoform of Dynein assembly factor with WD repeats 1  OS=Rattus norvegicus OX=10116 GN=Daw1 PE=4 SV=1 CANONICAL=Q5BK30-1"
            },
            "locus": {
                "chromosome": "9",
                "start_pos": 84472241,
                "end_pos": 84435587,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000103105.1",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000103105.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000095608.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000095608.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8L2QSV3-1",
            "url": "",
            "sequence": {
                "sequence": "MKLKSLLLRYYPPGIMLEYEKGGELKTKSIDLLELSPSTDVNTLVGEIQKVEPLITASRTKQVRLLVQRLQEKLRQHCDHNFYLFKVLRAHILPLTNVALNKAGSCFITGSYDRTCKVWDTASGEELHTLEGHRNVVYAIAFNNPYGDKIATGSFDKTCKLWSAETGKCYHTFRGHTAEIVCLSFNPQSTVVATGSMDTTAKLWDIQSGEEVVTLTGHLAEIISLSFDTSGDRIITGSFDHTVVVWDASTGRKVHTLIGHCAEISSALFSWDCSLILTGSMDKTCMLWDATSGKCVATLTGHDDEILDSCFDYTGKLIATASADGTARVYNATTRKCITKLEGHEGEISKISFNPQGNRLLTGSSDKTARIWDVQTGQCLQVLEGHTDEIFSCAFNYKGNIVITARTIPAGYGVDQRALLWSRADGVSDQDLEPPENKRAHFLCLLISCNLSMEQPALHFTDMTMKANGPSSFPDII",
                "length": 477,
                "header": "tr|A0A8L2QSV3-1|A0A8L2QSV3_RAT Computationally mapped isoform of Dynein assembly factor with WD repeats 1  OS=Rattus norvegicus OX=10116 GN=Daw1 PE=4 SV=1 CANONICAL=Q5BK30-1"
            },
            "locus": {
                "chromosome": "9",
                "start_pos": 84472431,
                "end_pos": 84435587,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000068236.4",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000068236.4"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000059421.3",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000059421.3"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q5BK30-1",
            "url": "",
            "sequence": {
                "sequence": "MKLKSLLLRYYPPGIMLEYEKGGELKTKSIDLLELSPSTDVNTLVGEIQKVEPLITASRTKQVRLLVQRLQEKLRQHCDHNFYLFKVLRAHILPLTNVALNKAGSCFITGSYDRTCKVWDTASGEELHTLEGHRNVVYAIAFNNPYGDKIATGSFDKTCKLWSAETGKCYHTFRGHTAEIVCLSFNPQSTVVATGSMDTTAKLWDIQSGEEVVTLTGHLAEIISLSFDTSGDRIITGSFDHTVVVWDASTGRKVHTLIGHCAEISSALFSWDCSLILTGSMDKTCMLWDATSGKCVATLTGHDDEILDSCFDYTGKLIATASADGTARVYNATTRKCITKLEGHEGEISKISFNPQGNRLLTGSSDKTARIWDVQTGQCLQVLEGHTDEIFSCAFNYKGNIVITGSKDNSCRIWR",
                "length": 415,
                "header": "sp|Q5BK30-1|DAW1_RAT Isoform 1 of Dynein assembly factor with WD repeat domains 1  OS=Rattus norvegicus OX=10116 GN=Daw1 PE=2 SV=1 CANONICAL=Q5BK30-1"
            },
            "locus": {}
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [
        {
            "id": "rno:363267",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:363267",
            "resource": "KEGG Pathway"
        }
    ],
    "orthologs": [
        {
            "uniprot_canonical_ac": "D3Z7A5-1",
            "protein_name": "Dynein assembly factor with WD repeat domains 1",
            "gene_name": "Daw1",
            "tax_id": 10090,
            "organism": "Mus musculus",
            "sequence": {
                "sequence": "MKLKSLLLRYYPPGIMLEYEKGGELKTKSIDLLELSPSTDVNTLVGEIQQAEPLITASRTKQVRLLVQRLQEKLRQHSDHNFYLFKVLRAHILPLTNVALNKAGSCFITGSYDRTCKVWDTASGEELHTLEGHKNVVYAIAFNNPYGDKIATGSFDKTCKLWSAETGKCYHTFRGHTAEIVCLSFNPQSTVVATGSMDTTAKLWDIQNGEEVVTLTGHLAEIISLSFDTSGDRIITGSFDHTVVVWDASTGRKVHTLIGHCAEISSALFNWDCSLILTGSMDKTCMLWDATSGKYVATLTGHDDEILDSCFDYTGKLIATASADGTARVYNATTRKCVTKLEGHEGEISKISFNPQGNRLLTGSSDKTARIWDVQTGQCLQVLEGHTDEIFSCAFNYKGNIVITGSKDNSCRIWR",
                "length": 415
            },
            "evidence": [
                {
                    "id": "45228533",
                    "url": "http://www.informatics.jax.org/homology/45228533",
                    "database": "MGI"
                }
            ],
            "common_name": "Mouse"
        },
        {
            "uniprot_canonical_ac": "Q8N136-1",
            "protein_name": "Dynein assembly factor with WD repeat domains 1",
            "gene_name": "DAW1",
            "tax_id": 9606,
            "organism": "Homo sapiens",
            "sequence": {
                "sequence": "MKLKSLLLRYYPPGIMLEYEKHGELKTKSIDLLDLGPSTDVSALVEEIQKAEPLLTASRTEQVKLLIQRLQEKLGQNSNHTFYLFKVLKAHILPLTNVALNKSGSCFITGSYDRTCKLWDTASGEELNTLEGHRNVVYAIAFNNPYGDKIATGSFDKTCKLWSVETGKCYHTFRGHTAEIVCLSFNPQSTLVATGSMDTTAKLWDIQNGEEVYTLRGHSAEIISLSFNTSGDRIITGSFDHTVVVWDADTGRKVNILIGHCAEISSASFNWDCSLILTGSMDKTCKLWDATNGKCVATLTGHDDEILDSCFDYTGKLIATASADGTARIFSAATRKCIAKLEGHEGEISKISFNPQGNHLLTGSSDKTARIWDAQTGQCLQVLEGHTDEIFSCAFNYKGNIVITGSKDNTCRIWR",
                "length": 415
            },
            "evidence": [
                {
                    "id": "45228533",
                    "url": "http://www.informatics.jax.org/homology/45228533",
                    "database": "MGI"
                }
            ],
            "common_name": "Human"
        }
    ],
    "go_annotation": {
        "categories": [
            {
                "name": "Biological Process",
                "total": 7,
                "go_terms": [
                    {
                        "name": "epithelial cilium movement involved in extracellular fluid movement",
                        "id": "GO:0003351",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003351",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q5BK30",
                                "url": "https://www.uniprot.org/uniprot/Q5BK30"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "heart development",
                        "id": "GO:0007507",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007507",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q5BK30",
                                "url": "https://www.uniprot.org/uniprot/Q5BK30"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "determination of left/right symmetry",
                        "id": "GO:0007368",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007368",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q5BK30",
                                "url": "https://www.uniprot.org/uniprot/Q5BK30"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "protein polyubiquitination",
                        "id": "GO:0000209",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000209",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q5BK30",
                                "url": "https://www.uniprot.org/uniprot/Q5BK30"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "outer dynein arm assembly",
                        "id": "GO:0036158",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0036158",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q5BK30",
                                "url": "https://www.uniprot.org/uniprot/Q5BK30"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "establishment of localization in cell",
                        "id": "GO:0051649",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051649",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q5BK30",
                                "url": "https://www.uniprot.org/uniprot/Q5BK30"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cerebrospinal fluid circulation",
                        "id": "GO:0090660",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090660",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q5BK30",
                                "url": "https://www.uniprot.org/uniprot/Q5BK30"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 3,
                "go_terms": [
                    {
                        "name": "extracellular region",
                        "id": "GO:0005576",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q5BK30",
                                "url": "https://www.uniprot.org/uniprot/Q5BK30"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cilium",
                        "id": "GO:0005929",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005929",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q5BK30",
                                "url": "https://www.uniprot.org/uniprot/Q5BK30"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "SCF ubiquitin ligase complex",
                        "id": "GO:0019005",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019005",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q5BK30",
                                "url": "https://www.uniprot.org/uniprot/Q5BK30"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Molecular Function",
                "total": 1,
                "go_terms": [
                    {
                        "name": "ubiquitin ligase-substrate adaptor activity",
                        "id": "GO:1990756",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990756",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q5BK30",
                                "url": "https://www.uniprot.org/uniprot/Q5BK30"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [
        {
            "start_pos": 331,
            "end_pos": 333,
            "annotation": "n_glycosylation_sequon"
        }
    ],
    "ptm_annotation": [],
    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
        },
        {
            "name": "homologset.mgi",
            "label": "MGI Homologs"
        }
    ],
    "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",
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                },
                {
                    "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": [
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                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
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                {
                    "field": "n_linked_glycans",
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                {
                    "field": "n_linked_glycan_sites",
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                {
                    "field": "o_linked_glycans",
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                {
                    "field": "o_linked_glycan_sites",
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                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_predicted",
            "table_stats": [
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                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
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                {
                    "field": "n_linked_glycans",
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                {
                    "field": "n_linked_glycan_sites",
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                {
                    "field": "o_linked_glycans",
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                {
                    "field": "o_linked_glycan_sites",
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                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_automatic_literature_mining",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
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                {
                    "field": "n_linked_glycans",
                    "count": 0
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                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
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                {
                    "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
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            ],
            "sort_fields": []
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        {
            "table_id": "snv_disease",
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                    "field": "total",
                    "count": 0
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        {
            "table_id": "snv_non_disease",
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                    "field": "total",
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            ],
            "sort_fields": []
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        {
            "table_id": "publication",
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                    "field": "total",
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            "sort_fields": []
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    ]
}