{
    "uniprot_canonical_ac": "Q8VHE6-1",
    "uniprot_ac": "Q8VHE6",
    "uniprot_id": "DYH5_MOUSE",
    "mass": {
        "chemical_mass": 527558.0,
        "monoisotopic_mass": 527558.0
    },
    "refseq": {},
    "gene_names": [
        {
            "name": "Dnah5",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/Q8VHE6",
            "id": "Q8VHE6"
        },
        {
            "name": "Dnahc5",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q8VHE6",
            "id": "Q8VHE6"
        }
    ],
    "protein_names": [
        {
            "name": "Dynein axonemal heavy chain 5",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "Q8VHE6"
        },
        {
            "name": "Axonemal beta dynein heavy chain 5",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q8VHE6"
        },
        {
            "name": "Ciliary dynein heavy chain 5",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q8VHE6"
        },
        {
            "name": "mDNAH5",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q8VHE6"
        }
    ],
    "function": [
        {
            "annotation": "Force generating protein of respiratory cilia. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Required for structural and functional integrity of the cilia of ependymal cells lining the brain ventricles.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q8VHE6",
                    "url": "https://www.uniprot.org/uniprot/Q8VHE6#function"
                },
                {
                    "database": "PubMed",
                    "id": "15269178",
                    "url": "https://glygen.org/publication/PubMed/15269178"
                }
            ]
        }
    ],
    "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:0110599",
            "recommended_name": {
                "id": "DOID:0110599",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0110599",
                "name": "primary ciliary dyskinesia 3",
                "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect, ciliary akinesia and variable occurence of situs inversus and has_material_basis_in homozygous or compound heterozygous mutation in the DNAH5 gene on chromosome 5p15."
            },
            "synonyms": [
                {
                    "id": "DOID:0110599",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110599",
                    "name": "CILD3",
                    "description": ""
                },
                {
                    "id": "DOID:0110599",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110599",
                    "name": "primary ciliary dyskinesia 3 with or without situs inversus",
                    "description": ""
                },
                {
                    "id": "MONDO:0012085",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012085",
                    "name": "primary ciliary dyskinesia 3",
                    "description": "Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the DNAH5 gene."
                },
                {
                    "id": "MONDO:0012085",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012085",
                    "name": "CILD3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012085",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012085",
                    "name": "DNAH5 primary ciliary dyskinesia",
                    "description": ""
                },
                {
                    "id": "MONDO:0012085",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012085",
                    "name": "ciliary dyskinesia, primary, type 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012085",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012085",
                    "name": "primary ciliary dyskinesia 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012085",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012085",
                    "name": "primary ciliary dyskinesia 3 with or without situs inversus",
                    "description": ""
                },
                {
                    "id": "MONDO:0012085",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012085",
                    "name": "primary ciliary dyskinesia caused by mutation in DNAH5",
                    "description": ""
                },
                {
                    "id": "MONDO:0012085",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012085",
                    "name": "primary ciliary dyskinesia type 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012085",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012085",
                    "name": "ciliary dyskinesia, primary, 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012085",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012085",
                    "name": "ciliary dyskinesia, primary, 3, with or without situs inversus",
                    "description": ""
                },
                {
                    "id": "MIM:608644",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/608644",
                    "name": "Ciliary dyskinesia, primary, 3",
                    "description": "Ciliary dyskinesia, primary, 3"
                }
            ],
            "evidence": [
                {
                    "id": "0110599",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110599"
                }
            ]
        },
        {
            "disease_id": "DOID:10754",
            "recommended_name": {
                "id": "DOID:10754",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:10754",
                "name": "otitis media",
                "description": "A otitis which involves inflammation of the middle ear."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "10754",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:10754"
                }
            ]
        },
        {
            "disease_id": "DOID:6419",
            "recommended_name": {
                "id": "DOID:6419",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:6419",
                "name": "tetralogy of Fallot",
                "description": ""
            },
            "synonyms": [
                {
                    "id": "DOID:6419",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:6419",
                    "name": "Ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle",
                    "description": ""
                },
                {
                    "id": "MONDO:0008542",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008542",
                    "name": "tetralogy of fallot",
                    "description": "Tetralogy of Fallot is a congenital cardiac malformation that consists of an interventricular communication, also known as a ventricular septal defect, obstruction of the right ventricular outflow tract, override of the ventricular septum by the aortic root, and right ventricular hypertrophy."
                },
                {
                    "id": "MONDO:0008542",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008542",
                    "name": "tetralogy of fallot",
                    "description": ""
                },
                {
                    "id": "MONDO:0008542",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008542",
                    "name": "ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle",
                    "description": ""
                },
                {
                    "id": "MONDO:0008542",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008542",
                    "name": "Fallot tetralogy",
                    "description": ""
                },
                {
                    "id": "MONDO:0008542",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008542",
                    "name": "TOF",
                    "description": ""
                },
                {
                    "id": "MONDO:0008542",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008542",
                    "name": "tetralogy of FALLOT",
                    "description": ""
                },
                {
                    "id": "MIM:187500",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/187500",
                    "name": "Tetralogy of Fallot",
                    "description": "Tetralogy of Fallot"
                }
            ],
            "evidence": [
                {
                    "id": "6419",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:6419"
                }
            ]
        },
        {
            "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": [
        {
            "evidence": [
                {
                    "id": "rs3389337558",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs3389337558"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ],
            "start_pos": 2061,
            "end_pos": 2061,
            "sequence_org": "I",
            "sequence_mut": "N",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (IFT->NFT).",
            "chr_id": "15",
            "chr_pos": "28327466",
            "ref_nt": "A",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "I2061",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs3389337590",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs3389337590"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ],
            "start_pos": 807,
            "end_pos": 807,
            "sequence_org": "F",
            "sequence_mut": "S",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NAF->NAS).",
            "chr_id": "15",
            "chr_pos": "28252728",
            "ref_nt": "C",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "F807",
            "keywords": [
                "ebi",
                "germline"
            ]
        }
    ],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Mus musculus",
            "taxid": 10090,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q8VHE6",
                    "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                }
            ],
            "common_name": "Mouse"
        }
    ],
    "gene": [
        {
            "name": "Dnah5",
            "url": "https://www.uniprot.org/uniprot/Q8VHE6",
            "locus": {
                "chromosome": "15",
                "start_pos": 28472198,
                "end_pos": 28203898,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "ENSMUSG00000022262",
                        "url": "https://www.ensembl.org/id/ENSMUSG00000022262"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "ENSMUSG00000022262",
            "url": "https://bgee.org/?page=gene&gene_id=ENSMUSG00000022262",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "Q8VHE6",
            "url": "https://www.ebi.ac.uk/intact/interactors/id:Q8VHE6*",
            "database": "IntAct",
            "categories": [
                "Other"
            ]
        },
        {
            "id": "IPR003593",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR003593",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR004273",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR004273",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR013594",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR013594",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR013602",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR013602",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR024317",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR024317",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR024743",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR024743",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR026983",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR026983",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR027417",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR027417",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR035699",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR035699",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR035706",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR035706",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR041228",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR041228",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR041466",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR041466",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR041589",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR041589",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR041658",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR041658",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR042219",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR042219",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR042222",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR042222",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR042228",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR042228",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR043157",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR043157",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR043160",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR043160",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "mmu:110082",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+mmu:110082",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "107718",
            "url": "http://www.informatics.jax.org/marker/MGI:107718",
            "database": "MGI",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "Q8VHE6",
            "url": "https://www.oglcnac.mcw.edu/search/?query_protein=Q8VHE6",
            "database": "O-GlcNAc Database",
            "categories": [
                "Glycoproteomics"
            ]
        },
        {
            "id": "FQKRDRY",
            "url": "https://omabrowser.org/oma/group/FQKRDRY/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "166463at2759",
            "url": "http://www.orthodb.org/?query=166463at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR46532",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR46532",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR46532:SF13",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR46532:SF13",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF03028",
            "url": "http://pfam.xfam.org/family/PF03028",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF08385",
            "url": "http://pfam.xfam.org/family/PF08385",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF08393",
            "url": "http://pfam.xfam.org/family/PF08393",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF12774",
            "url": "http://pfam.xfam.org/family/PF12774",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF12775",
            "url": "http://pfam.xfam.org/family/PF12775",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF12777",
            "url": "http://pfam.xfam.org/family/PF12777",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF12780",
            "url": "http://pfam.xfam.org/family/PF12780",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF12781",
            "url": "http://pfam.xfam.org/family/PF12781",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF17852",
            "url": "http://pfam.xfam.org/family/PF17852",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF17857",
            "url": "http://pfam.xfam.org/family/PF17857",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF18198",
            "url": "http://pfam.xfam.org/family/PF18198",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF18199",
            "url": "http://pfam.xfam.org/family/PF18199",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PR_Q8VHE6",
            "url": "http://purl.obolibrary.org/obo/PR_Q8VHE6",
            "database": "PRO",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q8VHE6",
            "url": "https://www.uniprot.org/uniprot/Q8VHE6",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q8VHE6-1",
            "url": "https://www.uniprot.org/uniprot/Q8VHE6-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MFRIGRRQLWKQSVTRVLTQRLKEEKEAKRARLDGRHDYLFAIVASCLDLNKPEVEDALLEGNQIERMDQLFAVGGLRHLMFYYQDVEGAEAGHCGSSGGVNPASGKMKKPKVFVTEGKDVALMGACVFFIRSDPSKAITPENIHREVSFNTLDTADGGLLNSVRRLLSDIFIPALRASSHGWGELEGLQDASSIRQEFLSSLEGFVGILSGAQNSLKEKVNLQKCDIIELKSLKEPTDYLALASNPETVEKVECCMRVWIKQMEQILAENSQLRKEADDVGPRAELEHWKQRLSRFNYLLDQLKSPDVKAALALLAAAKSKLLKVWRDTDIRITDAANEAKDNVKYLYTLEKCCDPLYSSDPVTMIDAIPTLINAIKMVYSISHYYNTSEKITSLFVKVTNQMISACKAHITNNGTATIWSQPQEIVMQKIAAVIKLKQGYQSCFQETKQKLKQNPSEKQFDFSEMYIFGKFETFHRRLAKIMDIFTTFKTYSVLQDSKIEGLEDMATKYQDIVAAIKKKEYNFLDQREMDFDQDYEEFCKRINELHNDLQRFMDITFEKIPSTRQALSTLKKFERLNIPNLGIEEKYQIIFQNFATDIDTISKLYTKQKYDPPLARNQPPIAGKILWARQLFHRLEQPMQLFQQHPFVLRTAEAKPVIRSYNRIAKVLLEFEVLYHRAWLQQIEEIHAGLEASLLVKAPGTGELFVNFDPQILVLFRETQCMSQLGLPVSPFAAALFQKRDMFKKNFSDMKMMLSEYERVKLKMPPAIEQLMFPHLARVDEALQPGLAVLTWTSLNIGGYLENAFAKIKDLELLLDRVNDLIEFRIHAILEEMSSMALCQLPQDDPLTCEEFLQMTKDLCVSGAQLLHFKSSLVEEAVNELINMLLDVDVPPEEAAENVCHENASPSGNTSGRREGHSEALASSFNAGASSLPLTATARKKKETEVLEEARELLSHFNHQNTDALLKVTRNTLEAIRRRIHFSHMINFRDSNDASKAKQNHLPIFRASVTLAIPNIAMTPALEDIQQTLNKAVECIISVPKGVRQWSSELLSKRKMHERKMAAVKNNEDSDSDAEVEENELQETLEIASINLPIPVQTQNYYKNISDNKEIVKLVSVLSTVISSTKKEVITSMDRFKRYNHIWQKEKEDTIMTFIAQNPLLPEFESRILYFQSLEQEINAEPEYIRVGSIALYTADLKLSLTAETKAWMAVIGRHCNRKYRAEMENILTVVEESQKKLSRPIKDLDDIRIAMAALKEIREQQISTDFQVGPIEESYALLNKYGLLVAKEEMDKVDTLRYAWEKLLARASDVQNELGALQPSFRKELISTVEVFLQDCQQFYLDYDLNGPMASGLKPQEASGRLIIFQNQFDNIYRKYITYTGGEELFGLPVTPYPQLLEIKRQLNLLQKIYSLYNNVIETVNSYQDTLWSDVNIEKINNELLEFQNRCRKLPRALKDWQAFLDLKKTIDDFSECCPLLEYMASNAMVERHWQRITALTGHSLDVGNETFKLRNIMEAPLLKYKEEIEDICISAVKERDIEQKLRQVINEWDNKTLTFSGFKTRGELLLRGDSTSEVIASMEDSLMLLGSLLSNRYNMPFKAQIQKWVQCLSNSTDIIENWMTVQNLWIYLEAVFVGGDIAKQLPKEAKRFSNIDKSWVKIMTRAHEIPNVVQCCVGDETMGQLLPHLLDQLEICQKSLTGYLEKKRLCFPRFFFVSDPALLEILGQASDSHTIQAHLLNVFDNIKTVKFHDKIYDRILSISSREGETIELDKPVMAEGNVEVWLNSLLEESQSSLHLVIRQAAANIQEPGFQLIEFLSSFPAQVGLLGIQMLWTRDSEEALRNAKFDKKIMQKTNQAFLELLNMLIEITTKDLSSMERVKYETLITIHVHQRDIFDDLCHMHVKSPTDFEWLKQCRFYFKEDSDKTMIHITDVAFIYQNEFLGCTDRLVITPLTDRCYITLAQALGMSMGGAPAGPAGTGKTETTKDMGRCLGKYVVVFNCSDQMDFRGLGRIFKGLAQSGSWGCFDEFNRIDLPVLSVAAQQISIILTCKKEHKKSFIFTDGDNVTMNPEFGLFLTMNPGYAGRQELPENLKINFRSVAMMVPDRQIIIRVKLASCGFIDNVVLARKFFTLYQLCEEQLSKQVHYDFGLRNILSVLRTLGAAKRASPTDTESTIVMRVLRDMNLSKLIDEDEPLFLSLIEDLFPNILLDKAGYPELETAISKQVEEAGLINHPPWKLKVIQLFETQRVRHGMMTLGPSGSGKTTCIHTLMKAMTDCGKPHREMRMNPKAITAPQMFGRLDVATNDWTDGIFSTLWRKTLKAKKGEHIWIVLDGPVDAIWIENLNSVLDDNKTLTLANGDRIPMAPNCKIVFEPHNIDNASPATVSRNGMVFMSSSVLDWSPILEGFLKRRSPQEAEILRQLYAETFPDLYRFSIQNLEFKMEVLEAFVITQSTHMLQGLIPPKEQAGEVDPEHLGRLFVFAMMWSVGAVLELEGRRRMELWLRSREGPTLHLPQLTDAGDTMFDYYVAPNGTWRHWSLCTPEYVYPPDTTPEYGSILVPNVDNVRTDFLIKTIAKQGKAVLLIGEQGTAKTVIIKGFMSKFDPESHMVKNLNFSSATTPVMFQRTIESYVDKRMGTTYGPPAGKKMAVFIDDLNMPVINEWGDQVTNEIVRQLMEQSGFYNLEKPGEFTSIVDIQFLAAMIHPGGGRNDIPQRLKRQFSIFNCTLPSDASMDKIFGVIGAGYYCAQRGFSEEVQDALIKLVPLTRRLWQMTKLKMLPTPAKFHYVFNLRDLSRIWQGMLNITSEVIKDTDELLRLWKHECKRVIADRFSMSSDVTWFDKAVVSLVEEEFGEEKAPVVDCGVDAYFVDFLRDAPEATGETPEEADAEMPKLYEPIASLNHLRERLSVFLQLYNESIRGTGMDMVFFIDAMVHLVKISRVIRTPRGNALLVGVGGSGKQSLTRLASFIAGYTSFQITLTRSYNTSNLMEDLKVLYRTAGQQGKGITFIFTDNEIKEESFLEYMNNVLSSGEVSNLFARDEIDEINSDLTPIMKKEHPRRPPTNDNLYEYFMSRVRGNLHIVLCFSPVGEKFRNRALKFPALISGCTIDWFSRWPKDALVAVSEHFLSSYTIDCTAEIKKELVQCMGSFQDGVAEKCADYFQRFRRSTHVTPKSYLSFIQGYKFIYEEKHMEVQSLANRMNTGLEKLKEASESVAALSKELAGKEKELQVANEKADTVLKEVTMKAQAAEKVKAEVQKVKDKAQAIVDSISKDKAIAEEKLEAAKPALEEAEAALQTIKPSDIATVRTLGRPPHLIMRIMDCVLLLFQRRVNAVKIDVDKGCTMPSWQESLKLMTAGNFLQNLQQFPKDTINEEVIEFLNPYFEMSDYNIETAKRVCGNVAGLCSWTKAMASFFSINKEVLPLKANLIVQENRHILAMQDLQKAQAELDAKQAELDVVQAEYEQAMAEKQTLLEDADRCRHKMQTASTLISGLAGEKERWTEQSKEFAAQTKRLVGDVLLATAFLSYSGPFNQEFRDLLLHDWKKEMKARKIPFGNGLNLNEMLIDAPTISEWNLQGLPNDDLSIQNGIIVTKASRYPLLIDPQTQGKIWIKNKESQNELQITSLNHKYFRNHLEDSLSLGRPLLIEDVGEELDPALDNVLEKNFIKTGSTFKVKVGDKEVDVMDGFKLYITTKLPNPAYTPEISARTSIIDFTVTVKGLEDQLLGRVILTEKQELEKERTHLLEDVTANKRRMKELEDNLLYRLTSTQGSLVEDESLIIVLSNTKKTAEEVTQKLEISGETEIQINSAREEYRPVATRGSILYFLITEMRLVNEMYQTSLRQFLGLFDLSLARSVKSPITSKRIANIIEHMTYEVFKYAARGLYEEHKFLFTLLLTLKIDIQRNLVKHEEFLTLIKGGASLDLKACPPKPSKWILDMTWLNLVELSKLKQFSDILDQISRNEKMWRVWFDKENPEEEPLPNAYDKSLDCFRRLLLIRSWCPDRTIAQARKYIMDSMGENYAEGVILDLEKTWEESDPRTPLICLLSMGSDPTDSIIALGKRLKIETRYVSMGQGQEVHARKLLHQTMANGGWVLLQNCHLGLDFLDELMDVVTETETVHDTFRLWITTEVHKQFPITLLQMSIKFANEPPQGLRAGLRRTYGGVSQDLLDVSVGAQWKPMLYAVAFLHSTVQERRKFGPLGWNIPYEFNQADFNATVQFIQNHLDDMDVKKGVSWTTVRYMIGEIQYGGRVTDDYDKRLLNTFAKVWFSENMFGPDFTFYQGYNIPKCSTVDGYLQYIQSLPAYDSPEVFGLHPNADITYQSKLAKDVLDTILGIQPKDSSGGGDETREAVVARLADDMLEKLPEDYSPFEVKERLQKMGPFQPMNIFLRQEIDRMQRVLSLVRSTLTELKLAVDGTIIMSENLRDALDCMFDARIPARWKKASWVSSTLGFWFTELLERNCQFTSWVSNGRPHCFWMTGFFNPQGFLTAMRQEITRANKGWALDNMVLCNEVTKFMKDDISAPPTEGVYVYGLYLEGAGWDKRNMKLIESKPKVLFELMPVIRIFAENNTARDPRLYCCPIYKKPVRTDLNYIAAVDLKTAQAPEHWVLRGVALLCDVK",
        "length": 4621,
        "header": "sp|Q8VHE6-1|DYH5_MOUSE Isoform 1 of Dynein axonemal heavy chain 5  OS=Mus musculus OX=10090 GN=Dnah5 PE=1 SV=2 CANONICAL=Q8VHE6-1"
    },
    "isoforms": [
        {
            "isoform_ac": "Q8VHE6-1",
            "url": "",
            "sequence": {
                "sequence": "MFRIGRRQLWKQSVTRVLTQRLKEEKEAKRARLDGRHDYLFAIVASCLDLNKPEVEDALLEGNQIERMDQLFAVGGLRHLMFYYQDVEGAEAGHCGSSGGVNPASGKMKKPKVFVTEGKDVALMGACVFFIRSDPSKAITPENIHREVSFNTLDTADGGLLNSVRRLLSDIFIPALRASSHGWGELEGLQDASSIRQEFLSSLEGFVGILSGAQNSLKEKVNLQKCDIIELKSLKEPTDYLALASNPETVEKVECCMRVWIKQMEQILAENSQLRKEADDVGPRAELEHWKQRLSRFNYLLDQLKSPDVKAALALLAAAKSKLLKVWRDTDIRITDAANEAKDNVKYLYTLEKCCDPLYSSDPVTMIDAIPTLINAIKMVYSISHYYNTSEKITSLFVKVTNQMISACKAHITNNGTATIWSQPQEIVMQKIAAVIKLKQGYQSCFQETKQKLKQNPSEKQFDFSEMYIFGKFETFHRRLAKIMDIFTTFKTYSVLQDSKIEGLEDMATKYQDIVAAIKKKEYNFLDQREMDFDQDYEEFCKRINELHNDLQRFMDITFEKIPSTRQALSTLKKFERLNIPNLGIEEKYQIIFQNFATDIDTISKLYTKQKYDPPLARNQPPIAGKILWARQLFHRLEQPMQLFQQHPFVLRTAEAKPVIRSYNRIAKVLLEFEVLYHRAWLQQIEEIHAGLEASLLVKAPGTGELFVNFDPQILVLFRETQCMSQLGLPVSPFAAALFQKRDMFKKNFSDMKMMLSEYERVKLKMPPAIEQLMFPHLARVDEALQPGLAVLTWTSLNIGGYLENAFAKIKDLELLLDRVNDLIEFRIHAILEEMSSMALCQLPQDDPLTCEEFLQMTKDLCVSGAQLLHFKSSLVEEAVNELINMLLDVDVPPEEAAENVCHENASPSGNTSGRREGHSEALASSFNAGASSLPLTATARKKKETEVLEEARELLSHFNHQNTDALLKVTRNTLEAIRRRIHFSHMINFRDSNDASKAKQNHLPIFRASVTLAIPNIAMTPALEDIQQTLNKAVECIISVPKGVRQWSSELLSKRKMHERKMAAVKNNEDSDSDAEVEENELQETLEIASINLPIPVQTQNYYKNISDNKEIVKLVSVLSTVISSTKKEVITSMDRFKRYNHIWQKEKEDTIMTFIAQNPLLPEFESRILYFQSLEQEINAEPEYIRVGSIALYTADLKLSLTAETKAWMAVIGRHCNRKYRAEMENILTVVEESQKKLSRPIKDLDDIRIAMAALKEIREQQISTDFQVGPIEESYALLNKYGLLVAKEEMDKVDTLRYAWEKLLARASDVQNELGALQPSFRKELISTVEVFLQDCQQFYLDYDLNGPMASGLKPQEASGRLIIFQNQFDNIYRKYITYTGGEELFGLPVTPYPQLLEIKRQLNLLQKIYSLYNNVIETVNSYQDTLWSDVNIEKINNELLEFQNRCRKLPRALKDWQAFLDLKKTIDDFSECCPLLEYMASNAMVERHWQRITALTGHSLDVGNETFKLRNIMEAPLLKYKEEIEDICISAVKERDIEQKLRQVINEWDNKTLTFSGFKTRGELLLRGDSTSEVIASMEDSLMLLGSLLSNRYNMPFKAQIQKWVQCLSNSTDIIENWMTVQNLWIYLEAVFVGGDIAKQLPKEAKRFSNIDKSWVKIMTRAHEIPNVVQCCVGDETMGQLLPHLLDQLEICQKSLTGYLEKKRLCFPRFFFVSDPALLEILGQASDSHTIQAHLLNVFDNIKTVKFHDKIYDRILSISSREGETIELDKPVMAEGNVEVWLNSLLEESQSSLHLVIRQAAANIQEPGFQLIEFLSSFPAQVGLLGIQMLWTRDSEEALRNAKFDKKIMQKTNQAFLELLNMLIEITTKDLSSMERVKYETLITIHVHQRDIFDDLCHMHVKSPTDFEWLKQCRFYFKEDSDKTMIHITDVAFIYQNEFLGCTDRLVITPLTDRCYITLAQALGMSMGGAPAGPAGTGKTETTKDMGRCLGKYVVVFNCSDQMDFRGLGRIFKGLAQSGSWGCFDEFNRIDLPVLSVAAQQISIILTCKKEHKKSFIFTDGDNVTMNPEFGLFLTMNPGYAGRQELPENLKINFRSVAMMVPDRQIIIRVKLASCGFIDNVVLARKFFTLYQLCEEQLSKQVHYDFGLRNILSVLRTLGAAKRASPTDTESTIVMRVLRDMNLSKLIDEDEPLFLSLIEDLFPNILLDKAGYPELETAISKQVEEAGLINHPPWKLKVIQLFETQRVRHGMMTLGPSGSGKTTCIHTLMKAMTDCGKPHREMRMNPKAITAPQMFGRLDVATNDWTDGIFSTLWRKTLKAKKGEHIWIVLDGPVDAIWIENLNSVLDDNKTLTLANGDRIPMAPNCKIVFEPHNIDNASPATVSRNGMVFMSSSVLDWSPILEGFLKRRSPQEAEILRQLYAETFPDLYRFSIQNLEFKMEVLEAFVITQSTHMLQGLIPPKEQAGEVDPEHLGRLFVFAMMWSVGAVLELEGRRRMELWLRSREGPTLHLPQLTDAGDTMFDYYVAPNGTWRHWSLCTPEYVYPPDTTPEYGSILVPNVDNVRTDFLIKTIAKQGKAVLLIGEQGTAKTVIIKGFMSKFDPESHMVKNLNFSSATTPVMFQRTIESYVDKRMGTTYGPPAGKKMAVFIDDLNMPVINEWGDQVTNEIVRQLMEQSGFYNLEKPGEFTSIVDIQFLAAMIHPGGGRNDIPQRLKRQFSIFNCTLPSDASMDKIFGVIGAGYYCAQRGFSEEVQDALIKLVPLTRRLWQMTKLKMLPTPAKFHYVFNLRDLSRIWQGMLNITSEVIKDTDELLRLWKHECKRVIADRFSMSSDVTWFDKAVVSLVEEEFGEEKAPVVDCGVDAYFVDFLRDAPEATGETPEEADAEMPKLYEPIASLNHLRERLSVFLQLYNESIRGTGMDMVFFIDAMVHLVKISRVIRTPRGNALLVGVGGSGKQSLTRLASFIAGYTSFQITLTRSYNTSNLMEDLKVLYRTAGQQGKGITFIFTDNEIKEESFLEYMNNVLSSGEVSNLFARDEIDEINSDLTPIMKKEHPRRPPTNDNLYEYFMSRVRGNLHIVLCFSPVGEKFRNRALKFPALISGCTIDWFSRWPKDALVAVSEHFLSSYTIDCTAEIKKELVQCMGSFQDGVAEKCADYFQRFRRSTHVTPKSYLSFIQGYKFIYEEKHMEVQSLANRMNTGLEKLKEASESVAALSKELAGKEKELQVANEKADTVLKEVTMKAQAAEKVKAEVQKVKDKAQAIVDSISKDKAIAEEKLEAAKPALEEAEAALQTIKPSDIATVRTLGRPPHLIMRIMDCVLLLFQRRVNAVKIDVDKGCTMPSWQESLKLMTAGNFLQNLQQFPKDTINEEVIEFLNPYFEMSDYNIETAKRVCGNVAGLCSWTKAMASFFSINKEVLPLKANLIVQENRHILAMQDLQKAQAELDAKQAELDVVQAEYEQAMAEKQTLLEDADRCRHKMQTASTLISGLAGEKERWTEQSKEFAAQTKRLVGDVLLATAFLSYSGPFNQEFRDLLLHDWKKEMKARKIPFGNGLNLNEMLIDAPTISEWNLQGLPNDDLSIQNGIIVTKASRYPLLIDPQTQGKIWIKNKESQNELQITSLNHKYFRNHLEDSLSLGRPLLIEDVGEELDPALDNVLEKNFIKTGSTFKVKVGDKEVDVMDGFKLYITTKLPNPAYTPEISARTSIIDFTVTVKGLEDQLLGRVILTEKQELEKERTHLLEDVTANKRRMKELEDNLLYRLTSTQGSLVEDESLIIVLSNTKKTAEEVTQKLEISGETEIQINSAREEYRPVATRGSILYFLITEMRLVNEMYQTSLRQFLGLFDLSLARSVKSPITSKRIANIIEHMTYEVFKYAARGLYEEHKFLFTLLLTLKIDIQRNLVKHEEFLTLIKGGASLDLKACPPKPSKWILDMTWLNLVELSKLKQFSDILDQISRNEKMWRVWFDKENPEEEPLPNAYDKSLDCFRRLLLIRSWCPDRTIAQARKYIMDSMGENYAEGVILDLEKTWEESDPRTPLICLLSMGSDPTDSIIALGKRLKIETRYVSMGQGQEVHARKLLHQTMANGGWVLLQNCHLGLDFLDELMDVVTETETVHDTFRLWITTEVHKQFPITLLQMSIKFANEPPQGLRAGLRRTYGGVSQDLLDVSVGAQWKPMLYAVAFLHSTVQERRKFGPLGWNIPYEFNQADFNATVQFIQNHLDDMDVKKGVSWTTVRYMIGEIQYGGRVTDDYDKRLLNTFAKVWFSENMFGPDFTFYQGYNIPKCSTVDGYLQYIQSLPAYDSPEVFGLHPNADITYQSKLAKDVLDTILGIQPKDSSGGGDETREAVVARLADDMLEKLPEDYSPFEVKERLQKMGPFQPMNIFLRQEIDRMQRVLSLVRSTLTELKLAVDGTIIMSENLRDALDCMFDARIPARWKKASWVSSTLGFWFTELLERNCQFTSWVSNGRPHCFWMTGFFNPQGFLTAMRQEITRANKGWALDNMVLCNEVTKFMKDDISAPPTEGVYVYGLYLEGAGWDKRNMKLIESKPKVLFELMPVIRIFAENNTARDPRLYCCPIYKKPVRTDLNYIAAVDLKTAQAPEHWVLRGVALLCDVK",
                "length": 4621,
                "header": "sp|Q8VHE6-1|DYH5_MOUSE Isoform 1 of Dynein axonemal heavy chain 5  OS=Mus musculus OX=10090 GN=Dnah5 PE=1 SV=2 CANONICAL=Q8VHE6-1"
            },
            "locus": {
                "chromosome": "15",
                "start_pos": 28470651,
                "end_pos": 28204125,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSMUST00000067048",
                        "url": "https://www.ensembl.org/id/ENSMUST00000067048"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSMUSP00000069751",
                        "url": "https://www.ensembl.org/id/ENSMUSP00000069751"
                    }
                ]
            }
        }
    ],
    "glycosylation": [
        {
            "glytoucan_ac": "G49108TO",
            "type": "O-linked",
            "subtype": "O-GlcNAcylation",
            "site_category": "reported_with_glycan",
            "site_seq": "T",
            "relation": "attached",
            "comment": "O-GlcNAcylation",
            "start_pos": 3668,
            "start_aa": "Thr",
            "end_pos": 3668,
            "end_aa": "Thr",
            "residue": "Thr",
            "site_lbl": "Thr3668",
            "evidence": [
                {
                    "id": "Q8VHE6",
                    "database": "O-GlcNAc Database",
                    "url": "https://www.oglcnac.mcw.edu/search/?query_protein=Q8VHE6"
                },
                {
                    "id": "34418053",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/34418053"
                }
            ]
        }
    ],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [
        "glycoprotein",
        "glycoprotein_reported_with_glycan"
    ],
    "publication": [
        {
            "title": "Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry.",
            "journal": "Nat. Genet.",
            "date": "2002",
            "authors": "Olbrich H, Haffner K, Kispert A, Volkel A, Volz A, Sasmaz G, Reinhardt R, Hennig S, Lehrach H, Konietzko N, Zariwala M, Noone PG, Knowles M, Mitchison HM, Meeks M, Chung EM, Hildebrandt F, Sudbrak R, Omran H",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q8VHE6",
                    "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "11788826",
                    "url": "https://glygen.org/publication/PubMed/11788826"
                }
            ]
        },
        {
            "title": "Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus.",
            "journal": "Hum. Mol. Genet.",
            "date": "2002",
            "authors": "Ibanez-Tallon I, Gorokhova S, Heintz N",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q8VHE6",
                    "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "11912187",
                    "url": "https://glygen.org/publication/PubMed/11912187"
                }
            ]
        },
        {
            "title": "Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation.",
            "journal": "Hum. Mol. Genet.",
            "date": "2004",
            "authors": "Ibanez-Tallon I, Pagenstecher A, Fliegauf M, Olbrich H, Kispert A, Ketelsen UP, North A, Heintz N, Omran H",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q8VHE6",
                    "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "15269178",
                    "url": "https://glygen.org/publication/PubMed/15269178"
                }
            ]
        },
        {
            "title": "O-GlcNAcylation Is Essential for Rapid Pomc Expression and Cell Proliferation in Corticotropic Tumor Cells.",
            "journal": "Endocrinology",
            "date": "2021",
            "authors": "Massman LJ, Pereckas M, Zwagerman NT, Olivier-Van Stichelen S",
            "evidence": [
                {
                    "database": "O-GlcNAc Database",
                    "id": "Q8VHE6",
                    "url": "https://www.oglcnac.mcw.edu/search/?query_protein=Q8VHE6"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "34418053",
                    "url": "https://glygen.org/publication/PubMed/34418053"
                }
            ]
        }
    ],
    "pathway": [
        {
            "id": "mmu:110082",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+mmu:110082",
            "resource": "KEGG Pathway"
        }
    ],
    "orthologs": [
        {
            "uniprot_canonical_ac": "Q8TE73-1",
            "protein_name": "Dynein axonemal heavy chain 5",
            "gene_name": "DNAH5",
            "tax_id": 9606,
            "organism": "Homo sapiens",
            "sequence": {
                "sequence": "MFRIGRRQLWKHSVTRVLTQRLKGEKEAKRALLDARHNYLFAIVASCLDLNKTEVEDAILEGNQIERIDQLFAVGGLRHLMFYYQDVEEAETGQLGSLGGVNLVSGKIKKPKVFVTEGNDVALTGVCVFFIRTDPSKAITPDNIHQEVSFNMLDAADGGLLNSVRRLLSDIFIPALRATSHGWGELEGLQDAANIRQEFLSSLEGFVNVLSGAQESLKEKVNLRKCDILELKTLKEPTDYLTLANNPETLGKIEDCMKVWIKQTEQVLAENNQLLKEADDVGPRAELEHWKKRLSKFNYLLEQLKSPDVKAVLAVLAAAKSKLLKTWREMDIRITDATNEAKDNVKYLYTLEKCCDPLYSSDPLSMMDAIPTLINAIKMIYSISHYYNTSEKITSLFVKVTNQIISACKAYITNNGTASIWNQPQDVVEEKILSAIKLKQEYQLCFHKTKQKLKQNPNAKQFDFSEMYIFGKFETFHRRLAKIIDIFTTLKTYSVLQDSTIEGLEDMATKYQGIVATIKKKEYNFLDQRKMDFDQDYEEFCKQTNDLHNELRKFMDVTFAKIQNTNQALRMLKKFERLNIPNLGIDDKYQLILENYGADIDMISKLYTKQKYDPPLARNQPPIAGKILWARQLFHRIQQPMQLFQQHPAVLSTAEAKPIIRSYNRMAKVLLEFEVLFHRAWLRQIEEIHVGLEASLLVKAPGTGELFVNFDPQILILFRETECMAQMGLEVSPLATSLFQKRDRYKRNFSNMKMMLAEYQRVKSKIPAAIEQLIVPHLAKVDEALQPGLAALTWTSLNIEAYLENTFAKIKDLELLLDRVNDLIEFRIDAILEEMSSTPLCQLPQEEPLTCEEFLQMTKDLCVNGAQILHFKSSLVEEAVNELVNMLLDVEVLSEEESEKISNENSVNYKNESSAKREEGNFDTLTSSINARANALLLTTVTRKKKETEMLGEEARELLSHFNHQNMDALLKVTRNTLEAIRKRIHSSHTINFRDSNSASNMKQNSLPIFRASVTLAIPNIVMAPALEDVQQTLNKAVECIISVPKGVRQWSSELLSKKKIQERKMAALQSNEDSDSDVEMGENELQDTLEIASVNLPIPVQTKNYYKNVSENKEIVKLVSVLSTIINSTKKEVITSMDCFKRYNHIWQKGKEEAIKTFITQSPLLSEFESQILYFQNLEQEINAEPEYVCVGSIALYTADLKFALTAETKAWMVVIGRHCNKKYRSEMENIFMLIEEFNKKLNRPIKDLDDIRIAMAALKEIREEQISIDFQVGPIEESYALLNRYGLLIAREEIDKVDTLHYAWEKLLARAGEVQNKLVSLQPSFKKELISAVEVFLQDCHQFYLDYDLNGPMASGLKPQEASDRLIMFQNQFDNIYRKYITYTGGEELFGLPATQYPQLLEIKKQLNLLQKIYTLYNSVIETVNSYYDILWSEVNIEKINNELLEFQNRCRKLPRALKDWQAFLDLKKIIDDFSECCPLLEYMASKAMMERHWERITTLTGHSLDVGNESFKLRNIMEAPLLKYKEEIEDICISAVKERDIEQKLKQVINEWDNKTFTFGSFKTRGELLLRGDSTSEIIANMEDSLMLLGSLLSNRYNMPFKAQIQKWVQYLSNSTDIIESWMTVQNLWIYLEAVFVGGDIAKQLPKEAKRFSNIDKSWVKIMTRAHEVPSVVQCCVGDETLGQLLPHLLDQLEICQKSLTGYLEKKRLCFPRFFFVSDPALLEILGQASDSHTIQAHLLNVFDNIKSVKFHEKIYDRILSISSQEGETIELDKPVMAEGNVEVWLNSLLEESQSSLHLVIRQAAANIQETGFQLTEFLSSFPAQVGLLGIQMIWTRDSEEALRNAKFDKKIMQKTNQAFLELLNTLIDVTTRDLSSTERVKYETLITIHVHQRDIFDDLCHMHIKSPMDFEWLKQCRFYFNEDSDKMMIHITDVAFIYQNEFLGCTDRLVITPLTDRCYITLAQALGMSMGGAPAGPAGTGKTETTKDMGRCLGKYVVVFNCSDQMDFRGLGRIFKGLAQSGSWGCFDEFNRIDLPVLSVAAQQISIILTCKKEHKKSFIFTDGDNVTMNPEFGLFLTMNPGYAGRQELPENLKINFRSVAMMVPDRQIIIRVKLASCGFIDNVVLARKFFTLYKLCEEQLSKQVHYDFGLRNILSVLRTLGAAKRANPMDTESTIVMRVLRDMNLSKLIDEDEPLFLSLIEDLFPNILLDKAGYPELEAAISRQVEEAGLINHPPWKLKVIQLFETQRVRHGMMTLGPSGAGKTTCIHTLMRAMTDCGKPHREMRMNPKAITAPQMFGRLDVATNDWTDGIFSTLWRKTLRAKKGEHIWIILDGPVDAIWIENLNSVLDDNKTLTLANGDRIPMAPNCKIIFEPHNIDNASPATVSRNGMVFMSSSILDWSPILEGFLKKRSPQEAEILRQLYTESFPDLYRFCIQNLEYKMEVLEAFVITQSINMLQGLIPLKEQGGEVSQAHLGRLFVFALLWSAGAALELDGRRRLELWLRSRPTGTLELPPPAGPGDTAFDYYVAPDGTWTHWNTRTQEYLYPSDTTPEYGSILVPNVDNVRTDFLIQTIAKQGKAVLLIGEQGTAKTVIIKGFMSKYDPECHMIKSLNFSSATTPLMFQRTIESYVDKRMGTTYGPPAGKKMTVFIDDVNMPIINEWGDQVTNEIVRQLMEQNGFYNLEKPGEFTSIVDIQFLAAMIHPGGGRNDIPQRLKRQFSIFNCTLPSEASVDKIFGVIGVGHYCTQRGFSEEVRDSVTKLVPLTRRLWQMTKIKMLPTPAKFHYVFNLRDLSRVWQGMLNTTSEVIKEPNDLLKLWKHECKRVIADRFTVSSDVTWFDKALVSLVEEEFGEEKKLLVDCGIDTYFVDFLRDAPEAAGETSEEADAETPKIYEPIESFSHLKERLNMFLQLYNESIRGAGMDMVFFADAMVHLVKISRVIRTPQGNALLVGVGGSGKQSLTRLASFIAGYVSFQITLTRSYNTSNLMEDLKVLYRTAGQQGKGITFIFTDNEIKDESFLEYMNNVLSSGEVSNLFARDEIDEINSDLASVMKKEFPRCLPTNENLHDYFMSRVRQNLHIVLCFSPVGEKFRNRALKFPALISGCTIDWFSRWPKDALVAVSEHFLTSYDIDCSLEIKKEVVQCMGSFQDGVAEKCVDYFQRFRRSTHVTPKSYLSFIQGYKFIYGEKHVEVRTLANRMNTGLEKLKEASESVAALSKELEAKEKELQVANDKADMVLKEVTMKAQAAEKVKAEVQKVKDRAQAIVDSISKDKAIAEEKLEAAKPALEEAEAALQTIRPSDIATVRTLGRPPHLIMRIMDCVLLLFQRKVSAVKIDLEKSCTMPSWQESLKLMTAGNFLQNLQQFPKDTINEEVIEFLSPYFEMPDYNIETAKRVCGNVAGLCSWTKAMASFFSINKEVLPLKANLVVQENRHLLAMQDLQKAQAELDDKQAELDVVQAEYEQAMTEKQTLLEDAERCRHKMQTASTLISGLAGEKERWTEQSQEFAAQTKRLVGDVLLATAFLSYSGPFNQEFRDLLLNDWRKEMKARKIPFGKNLNLSEMLIDAPTISEWNLQGLPNDDLSIQNGIIVTKASRYPLLIDPQTQGKIWIKNKESRNELQITSLNHKYFRNHLEDSLSLGRPLLIEDVGEELDPALDNVLERNFIKTGSTFKVKVGDKEVDVLDGFRLYITTKLPNPAYTPEISARTSIIDFTVTMKGLEDQLLGRVILTEKQELEKERTHLMEDVTANKRRMKELEDNLLYRLTSTQGSLVEDESLIVVLSNTKRTAEEVTQKLEISAETEVQINSAREEYRPVATRGSILYFLITEMRLVNEMYQTSLRQFLGLFDLSLARSVKSPITSKRIANIIEHMTYEVYKYAARGLYEEHKFLFTLLLTLKIDIQRNRVKHEEFLTLIKGGASLDLKACPPKPSKWILDITWLNLVELSKLRQFSDVLDQISRNEKMWKIWFDKENPEEEPLPNAYDKSLDCFRRLLLIRSWCPDRTIAQARKYIVDSMGEKYAEGVILDLEKTWEESDPRTPLICLLSMGSDPTDSIIALGKRLKIETRYVSMGQGQEVHARKLLQQTMANGGWALLQNCHLGLDFMDELMDIIIETELVHDAFRLWMTTEAHKQFPITLLQMSIKFANDPPQGLRAGLKRTYSGVSQDLLDVSSGSQWKPMLYAVAFLHSTVQERRKFGALGWNIPYEFNQADFNATVQFIQNHLDDMDVKKGVSWTTIRYMIGEIQYGGRVTDDYDKRLLNTFAKVWFSENMFGPDFSFYQGYNIPKCSTVDNYLQYIQSLPAYDSPEVFGLHPNADITYQSKLAKDVLDTILGIQPKDTSGGGDETREAVVARLADDMLEKLPPDYVPFEVKERLQKMGPFQPMNIFLRQEIDRMQRVLSLVRSTLTELKLAIDGTIIMSENLRDALDCMFDARIPAWWKKASWISSTLGFWFTELIERNSQFTSWVFNGRPHCFWMTGFFNPQGFLTAMRQEITRANKGWALDNMVLCNEVTKWMKDDISAPPTEGVYVYGLYLEGAGWDKRNMKLIESKPKVLFELMPVIRIYAENNTLRDPRFYSCPIYKKPVRTDLNYIAAVDLRTAQTPEHWVLRGVALLCDVK",
                "length": 4624
            },
            "evidence": [
                {
                    "id": "Q8VHE6",
                    "url": "https://omabrowser.org/oma/group/Q8VHE6/",
                    "database": "OMA"
                }
            ],
            "common_name": "Human"
        }
    ],
    "go_annotation": {
        "categories": [
            {
                "name": "Biological Process",
                "total": 9,
                "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": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "heart development",
                        "id": "GO:0007507",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007507",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "flagellated sperm motility",
                        "id": "GO:0030317",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030317",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cilium assembly",
                        "id": "GO:0060271",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060271",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "determination of left/right symmetry",
                        "id": "GO:0007368",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007368",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "lateral ventricle development",
                        "id": "GO:0021670",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0021670",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cilium movement",
                        "id": "GO:0003341",
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                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
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                        ],
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                    },
                    {
                        "name": "outer dynein arm assembly",
                        "id": "GO:0036158",
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                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "establishment of localization in cell",
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                                "database": "UniProtKB",
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                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Molecular Function",
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                        "name": "ATP binding",
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                        ],
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                    },
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                                "id": "Q8VHE6",
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                        ],
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                    },
                    {
                        "name": "minus-end-directed microtubule motor activity",
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                    {
                        "name": "dynein light intermediate chain binding",
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                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "dynein intermediate chain binding",
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                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
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                        "name": "extracellular region",
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                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
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                                "id": "Q8VHE6",
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                            }
                        ],
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                    },
                    {
                        "name": "cytoplasm",
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                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
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                        ],
                        "pmid": ""
                    },
                    {
                        "name": "microtubule",
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                            {
                                "database": "UniProtKB",
                                "id": "Q8VHE6",
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                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "motile cilium",
                        "id": "GO:0031514",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031514",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "axoneme",
                        "id": "GO:0005930",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005930",
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                            {
                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "axonemal dynein complex",
                        "id": "GO:0005858",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005858",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "outer dynein arm",
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                            {
                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "9+2 motile cilium",
                        "id": "GO:0097729",
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                            {
                                "database": "UniProtKB",
                                "id": "Q8VHE6",
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                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "9+0 motile cilium",
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                            {
                                "database": "UniProtKB",
                                "id": "Q8VHE6",
                                "url": "https://www.uniprot.org/uniprot/Q8VHE6"
                            }
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                        "pmid": ""
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                ]
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