{ "uniprot_canonical_ac": "A0A0R4IWI7-1", "uniprot_ac": "A0A0R4IWI7", "uniprot_id": "A0A0R4IWI7_DANRE", "mass": { "chemical_mass": 117738.0, "monoisotopic_mass": 117738.0 }, "refseq": { "ac": "NP_001186705", "name": "kinesin family member 5Aa", "summary": "", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001186705" }, "gene_names": [ { "name": "kif5aa", "resource": "UniProtKB", "type": "recommended", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7", "id": "A0A0R4IWI7" }, { "name": "kif5a; si:ch211-166e11.4; vertigo; vrt; wu:fj61a10", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001186705", "id": "NP_001186705" }, { "name": "kif5aa", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001186705", "id": "NP_001186705" }, { "name": "kif5a", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7", "id": "A0A0R4IWI7" }, { "name": "si:ch211-166e11.4", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7", "id": "A0A0R4IWI7" }, { "name": "vertigo", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7", "id": "A0A0R4IWI7" }, { "name": "vrt", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7", "id": "A0A0R4IWI7" }, { "name": "wu:fj61a10", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7", "id": "A0A0R4IWI7" } ], "protein_names": [ { "name": "Kinesin family member 5A, a", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7/entry#names_and_taxonomy", "id": "A0A0R4IWI7" }, { "name": "Kinesin family member 5Aa", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7/entry#names_and_taxonomy", "id": "A0A0R4IWI7" }, { "name": "kinesin family member 5Aa", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001186705", "id": "NP_001186705" } ], "function": [ { "annotation": "##Evidence-Data-START## Transcript exon combination :: GFIL01014007.1, SRR26395015.206512.1 [ECO:0000332] RNAseq introns :: mixed sample support SAMEA3505370, SAMEA3505371 [ECO:0006172] ##Evidence-Data-END## VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from BC095088.1 and JBMGRA010000009.1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.", "evidence": [ { "database": "RefSeq", "id": "NP_001186705", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001186705" } ] }, { "annotation": "Deletion of a kinesin I motor unmasks a mechanism of homeostatic axon-branching control by neurotrophin-3. Publication Status: Online-Only", "evidence": [ { "database": "RefSeq", "id": "NP_001186705", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001186705" }, { "database": "PubMed", "id": "26076409", "url": "https://glygen.org/publication/PubMed/26076409" } ] }, { "annotation": "Our results shed light on Kinesin complexity and reveal determinants of specific Kif5A functions in mitochondrial transport, adaptor binding, and axonal maintenance.", "evidence": [ { "database": "RefSeq", "id": "NP_001186705", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001186705" }, { "database": "PubMed", "id": "25355224", "url": "https://glygen.org/publication/PubMed/25355224" } ] } ], "disease": [ { "disease_id": "DOID:0081379", "recommended_name": { "id": "DOID:0081379", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0081379", "name": "amyotrophic lateral sclerosis type 25", "description": "An amyotrophic lateral sclerosis that is characterized by rapidly progressive muscle weakness and death due to respiratory failure and that has_material_basis_in heterozygous mutation in the KIF5A gene on chromosome 12q13. ALS25 may have a lower median age at onset (46.5 years) and longer median survival (10 years) than that found in epidemiologic studies (62.5 years and 20 to 30 months, respectively)." }, "synonyms": [ { "id": "MONDO:0060670", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0060670", "name": "amyotrophic lateral sclerosis, susceptibility to, 25", "description": "" }, { "id": "MONDO:0060670", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0060670", "name": "amyotrophic lateral sclerosis, susceptibility to, 25", "description": "" }, { "id": "MONDO:0060670", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0060670", "name": "ALS25", "description": "" }, { "id": "MIM:617921", "resource": "MIM", "url": "https://www.omim.org/entry/617921", "name": "Amyotrophic lateral sclerosis 25", "description": "Amyotrophic lateral sclerosis 25" } ], "unlinked_id_list": [], "evidence": [ { "id": "0081379", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:0081379" } ] }, { "disease_id": "DOID:0110763", "recommended_name": { "id": "DOID:0110763", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110763", "name": "hereditary spastic paraplegia 10", "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF5A gene on chromosome 12q13." }, "synonyms": [ { "id": "DOID:0110763", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110763", "name": "SPG10", "description": "" }, { "id": "DOID:0110763", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110763", "name": "autosomal dominant spastic paraplegia 10", "description": "" }, { "id": "DOID:0110763", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110763", "name": "autosomal dominant spastic paraplegia type 10", "description": "" }, { "id": "MONDO:0011408", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011408", "name": "hereditary spastic paraplegia 10", "description": "Autosomal dominant spastic paraplegia type 10 (SPG10) is a rare type of hereditary spastic paraplegia that can present as either a pure form of spastic paraplegia with lower limb spasticity, hyperreflexia and extensor plantar responses, presenting in childhood or adolescence, or as a complex phenotype associated with additional manifestations including peripheral neuropathy with upper limb amyotrophy, moderate intellectual disability and parkinsonism. Deafness and retinitis pigmentosa were reported in one case." }, { "id": "MONDO:0011408", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011408", "name": "KIF5A hereditary spastic paraplegia", "description": "" }, { "id": "MONDO:0011408", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011408", "name": "SPG10", "description": "" }, { "id": "MONDO:0011408", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011408", "name": "autosomal dominant spastic paraplegia 10", "description": "" }, { "id": "MONDO:0011408", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011408", "name": "autosomal dominant spastic paraplegia type 10", "description": "" }, { "id": "MONDO:0011408", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011408", "name": "hereditary spastic paraplegia caused by mutation in KIF5A", "description": "" }, { "id": "MONDO:0011408", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011408", "name": "hereditary spastic paraplegia type 10", "description": "" }, { "id": "MONDO:0011408", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011408", "name": "autosomal dominant spastic paraplegia", "description": "" }, { "id": "MONDO:0011408", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011408", "name": "spastic paraplegia 10", "description": "" }, { "id": "MONDO:0011408", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011408", "name": "spastic paraplegia 10 with or without peripheral neuropathy", "description": "" }, { "id": "MONDO:0011408", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011408", "name": "spastic paraplegia 10, autosomal dominant", "description": "" }, { "id": "MIM:604187", "resource": "MIM", "url": "https://www.omim.org/entry/604187", "name": "Spastic paraplegia 10, autosomal dominant", "description": "Spastic paraplegia 10, autosomal dominant" } ], "unlinked_id_list": [], "evidence": [ { "id": "0110763", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:0110763" } ] }, { "disease_id": "DOID:10283", "recommended_name": { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "prostate cancer", "description": "A male reproductive organ cancer that is located_in the prostate." }, "synonyms": [ { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "NGP - new growth of prostate", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "hereditary prostate cancer", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "malignant tumor of the prostate", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "prostate cancer, familial", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "prostate neoplasm", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "prostatic cancer", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "prostatic neoplasm", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "tumor of the prostate", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "prostate cancer, hereditary, 9", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "prostate cancer, hereditary, 9", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "prostate cancer, hereditary, type 9", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "HPC9", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "prostate cancer, hereditary, 12", "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene." }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "EHBP1 familial prostate cancer", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "familial prostate cancer caused by mutation in EHBP1", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "prostate cancer, hereditary, 12", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "prostate cancer, hereditary, type 12", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "HPC12", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "prostate cancer, hereditary, 5", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "prostate cancer, hereditary, 5", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "prostate cancer, hereditary, type 5", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "HPC5", "description": "" }, { "id": "MONDO:0012093", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012093", "name": "prostate cancer, hereditary, 3", "description": "" }, { "id": "MONDO:0012093", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012093", "name": "prostate cancer, hereditary, 3", "description": "" }, { "id": "MONDO:0012093", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012093", "name": "prostate cancer, hereditary, type 3", "description": "" }, { "id": "MONDO:0012093", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012093", "name": "prostate cancer, susceptibility to, 3", "description": "" }, { "id": "MONDO:0012093", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012093", "name": "HPC3", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, type 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, susceptibility to, 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "HPC4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, on chromosome 7", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "prostate cancer, hereditary, 13", "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene." }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "MSMB familial prostate cancer", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "familial prostate cancer caused by mutation in MSMB", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "prostate cancer, hereditary, 13", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "prostate cancer, hereditary, type 13", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "HPC13", "description": "" }, { "id": "MONDO:0011270", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011270", "name": "prostate cancer, hereditary, 8", "description": "" }, { "id": "MONDO:0011270", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011270", "name": "prostate cancer, hereditary, 8", "description": "" }, { "id": "MONDO:0011270", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011270", "name": "prostate cancer, hereditary, type 8", "description": "" }, { "id": "MONDO:0011270", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011270", "name": "HPC8", "description": "" }, { "id": "MONDO:0011270", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011270", "name": "predisposing for prostate cancer", "description": "" }, { "id": "MONDO:0011270", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011270", "name": "prostate cancer, susceptibility to", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, hereditary, 6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, hereditary, 6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, hereditary, type 6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "HPC6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, susceptibility to", "description": "" }, { "id": "MONDO:0012620", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012620", "name": "prostate cancer, hereditary, 10", "description": "" }, { "id": "MONDO:0012620", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012620", "name": "HPC10", "description": "" }, { "id": "MONDO:0012620", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012620", "name": "prostate cancer, hereditary, 10", "description": "" }, { "id": "MONDO:0700275", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0700275", "name": "prostate cancer, hereditary", "description": "An instance of prostate cancer that is caused by an inherited genomic modification in an individual. Familial prostate cancer (FPC) is a malignant tumor of the prostate with an early onset. FPC is either asymptomatic or causes mictionary symptoms, erectile dysfunction, bone pain, venous compression and infectious or inflammatory syndrome (for the metastatic forms). It is also characterized by familial antecedents." }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "prostate cancer, hereditary, 7", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "HPC7", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "prostate cancer, hereditary, 7", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "prostate cancer aggressiveness", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "prostate cancer, hereditary, 1", "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the RNASEL gene." }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "RNASEL familial prostate cancer", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "familial prostate cancer caused by mutation in RNASEL", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "prostate cancer 1", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "prostate cancer, hereditary, 1", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "prostate cancer, hereditary, type 1", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "HPC1", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "Prca1", "description": "" }, { "id": "MONDO:0012768", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012768", "name": "prostate cancer, hereditary, 11", "description": "" }, { "id": "MONDO:0012768", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012768", "name": "HPC11", "description": "" }, { "id": "MONDO:0012768", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012768", "name": "prostate cancer, hereditary, 11", "description": "" }, { "id": "MONDO:0012769", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012769", "name": "prostate cancer, hereditary, 14", "description": "" }, { "id": "MONDO:0012769", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012769", "name": "HPC14", "description": "" }, { "id": "MONDO:0012769", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012769", "name": "prostate cancer, hereditary, 14", "description": "" }, { "id": "MONDO:0012770", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012770", "name": "prostate cancer, hereditary, 15", "description": "" }, { "id": "MONDO:0012770", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012770", "name": "HPC15", "description": "" }, { "id": "MONDO:0012770", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012770", "name": "prostate cancer, hereditary, 15", "description": "" }, { "id": "MONDO:0010257", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010257", "name": "prostate cancer, hereditary, X-linked 1", "description": "" }, { "id": "MONDO:0010257", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010257", "name": "HPCX1", "description": "" }, { "id": "MONDO:0010257", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010257", "name": "prostate cancer, hereditary, X-linked 1", "description": "" }, { "id": "MONDO:0010257", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010257", "name": "prostate cancer susceptibility, X-linked", "description": "" }, { "id": "MONDO:0010405", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010405", "name": "prostate cancer, hereditary, X-linked 2", "description": "" }, { "id": "MONDO:0010405", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010405", "name": "HPCX2", "description": "" }, { "id": "MONDO:0010405", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010405", "name": "prostate cancer, hereditary, X-linked 2", "description": "" }, { "id": "MIM:610997", "resource": "MIM", "url": "https://www.omim.org/entry/610997", "name": "Prostate cancer, hereditary, 9", "description": "Prostate cancer, hereditary, 9" }, { "id": "MIM:611868", "resource": "MIM", "url": "https://www.omim.org/entry/611868", "name": "Prostate cancer, hereditary, 12", "description": "Prostate cancer, hereditary, 12" }, { "id": "MIM:611928", "resource": "MIM", "url": "https://www.omim.org/entry/611928", "name": "Prostate cancer, hereditary, 13", "description": "Prostate cancer, hereditary, 13" }, { "id": "MIM:176807", "resource": "MIM", "url": "https://www.omim.org/entry/176807", "name": "Prostate cancer", "description": "Prostate cancer" }, { "id": "MIM:601518", "resource": "MIM", "url": "https://www.omim.org/entry/601518", "name": "Prostate cancer, hereditary, 1", "description": "Prostate cancer, hereditary, 1" }, { "id": "MIM:611955", "resource": "MIM", "url": "https://www.omim.org/entry/611955", "name": "Prostate cancer, hereditary, 11", "description": "Prostate cancer, hereditary, 11" } ], "unlinked_id_list": [], "evidence": [ { "id": "10283", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:10283" } ] }, { "disease_id": "DOID:2377", "recommended_name": { "id": "DOID:2377", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2377", "name": "multiple sclerosis", "description": "A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring." }, "synonyms": [ { "id": "DOID:2377", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2377", "name": "Generalized multiple sclerosis", "description": "" }, { "id": "DOID:2377", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2377", "name": "insular sclerosis", "description": "" }, { "id": "MONDO:0012957", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012957", "name": "multiple sclerosis, susceptibility to, 3", "description": "" }, { "id": "MONDO:0012957", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012957", "name": "MS3", "description": "" }, { "id": "MONDO:0012957", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012957", "name": "multiple sclerosis, susceptibility to, 3", "description": "" }, { "id": "MONDO:0012956", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012956", "name": "multiple sclerosis, susceptibility to, 2", "description": "" }, { "id": "MONDO:0012956", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012956", "name": "MS2", "description": "" }, { "id": "MONDO:0012956", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012956", "name": "multiple sclerosis, susceptibility to, 2", "description": "" }, { "id": "MONDO:0012958", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012958", "name": "multiple sclerosis, susceptibility to, 4", "description": "" }, { "id": "MONDO:0012958", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012958", "name": "MS4", "description": "" }, { "id": "MONDO:0012958", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012958", "name": "multiple sclerosis, susceptibility to, 4", "description": "" }, { "id": "MIM:612595", "resource": "MIM", "url": "https://www.omim.org/entry/612595", "name": "Multiple sclerosis 3", "description": "Multiple sclerosis 3" } ], "unlinked_id_list": [], "evidence": [ { "id": "2377", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:2377" } ] }, { "disease_id": "DOID:7148", "recommended_name": { "id": "DOID:7148", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:7148", "name": "rheumatoid arthritis", "description": "An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint." }, "synonyms": [ { "id": "DOID:7148", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:7148", "name": "Arthritis or polyarthritis, rheumatic", "description": "" }, { "id": "DOID:7148", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:7148", "name": "atrophic Arthritis", "description": "" }, { "id": "MONDO:0008383", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008383", "name": "rheumatoid arthritis", "description": "A chronic, systemic autoimmune disorder characterized by inflammation in the synovial membranes and articular surfaces. It manifests primarily as a symmetric, erosive polyarthritis that spares the axial skeleton and is typically associated with the presence in the serum of rheumatoid factor." }, { "id": "MONDO:0008383", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008383", "name": "atrophic arthritis", "description": "" }, { "id": "MONDO:0008383", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008383", "name": "RA", "description": "" }, { "id": "MONDO:0008383", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008383", "name": "arthritis or polyarthritis, rheumatic", "description": "" }, { "id": "MONDO:0008383", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008383", "name": "arthritis, rheumatoid", "description": "" }, { "id": "MONDO:0008383", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008383", "name": "autoimmune arthritis", "description": "" }, { "id": "MONDO:0008383", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008383", "name": "rheumatoid arthritis", "description": "" }, { "id": "MONDO:0008383", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008383", "name": "rheumatoid arthritis, progression of", "description": "" }, { "id": "MONDO:0008383", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008383", "name": "rheumatoid arthritis, susceptibility to", "description": "" }, { "id": "MIM:180300", "resource": "MIM", "url": "https://www.omim.org/entry/180300", "name": "Rheumatoid arthritis", "description": "Rheumatoid arthritis" } ], "unlinked_id_list": [], "evidence": [ { "id": "7148", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:7148" } ] }, { "disease_id": "DOID:7596", "recommended_name": { "id": "DOID:7596", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:7596", "name": "asbestos-related lung carcinoma", "description": "" }, "synonyms": [], "unlinked_id_list": [], "evidence": [ { "id": "7596", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:7596" } ] } ], "snv": [], "mutagenesis": [], "expression_tissue": [], "expression_disease": [], "species": [ { "name": "Danio rerio", "taxid": 7955, "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "common_name": "Zebrafish", "glygen_name": "Zebrafish", "reference_species": "Danio rerio [7955]" } ], "gene": [ { "name": "kif5aa", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7", "locus": {} } ], "crossref": [ { "id": "ZFIN:ZDB-GENE-070912-141", "url": "https://alliancegenome.org/gene/ZFIN:ZDB-GENE-070912-141", "database": "AGR", "categories": [ "Protein Classification" ] }, { "id": "ENSDARG00000098936", "url": "https://bgee.org/?page=gene&gene_id=ENSDARG00000098936", "database": "Bgee", "categories": [ "Gene Expression" ] }, { "id": "cd01369", "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd01369", "database": "CDD", "categories": [ "Protein Classification" ] }, { "id": "cd23649", "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd23649", "database": "CDD", "categories": [ "Protein Classification" ] }, { "id": "566086", "url": "https://www.ncbi.nlm.nih.gov/gene/566086", "database": "GeneID", "categories": [ "Genome Annotation" ] }, { "id": "IPR001752", "url": "https://www.ebi.ac.uk/interpro/entry/IPR001752", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR019821", "url": "https://www.ebi.ac.uk/interpro/entry/IPR019821", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR027417", "url": "https://www.ebi.ac.uk/interpro/entry/IPR027417", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR027640", "url": "https://www.ebi.ac.uk/interpro/entry/IPR027640", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR036961", "url": "https://www.ebi.ac.uk/interpro/entry/IPR036961", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "dre:566086", "url": "https://www.genome.jp/dbget-bin/www_bget?dre:566086", "database": "KEGG Pathway", "categories": [ "Enzyme and Pathway" ] }, { "id": "CGSMVDD", "url": "https://omabrowser.org/oma/group/CGSMVDD/", "database": "OMA", "categories": [ "Protein Classification" ] }, { "id": "A0A0R4IWI7", "url": "https://www.orthodb.org/?gene=A0A0R4IWI7", "database": "OrthoDB", "categories": [ "Protein Classification" ] }, { "id": "PTHR47968", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR47968", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PTHR47968:SF36", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR47968:SF36", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PF00225", "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF00225", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "NP_001186705", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001186705", "database": "RefSeq", "categories": [ "Protein" ] }, { "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A0R4IWI7-1", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "ZDB-GENE-070912-141", "url": "https://zfin.org/ZDB-GENE-070912-141", "database": "ZFIN", "categories": [ "Protein", "Organism-specific" ] } ], "sequence": { "sequence": "MTDAAAECNIKVLCRFRPLNQAEILRGDKFLPTFQGDDTVIIGGKSYAFDRVFPTNTTQEQVYNTCAKQIVKDVLGGYNGTIFAYGQTSSGKTHTMEGNLHDPQQMGIIPRIAEDIFNHIFSMDENLEFHIKVSYFEIYMEKIRDLLDVTKTNLSVHEDKNRVPYVKGCTERFVSSPEEVMDVIDEGKSNRHVAVTNMNEHSSRSHSIFLINIKQEHVETEQKLCGKLYLVDLAGSEKVSKTGAAGAVLDEAKNINKSLSALGNVISALAEGTKSHVPYRDSKMTRILQDSLGGNCRTTMFICCSPSSYNDAETKSTLMFGQRAKTIKNTASINLELTAEQWKRKYEKEKEKNKSLRDSMQRLELELRRWRNGEKVPETEQTDADVVKLDVSEETSLDNEKSCERQRERERDSDTSSIVVRISEEERQKYEEEIRKLYRQLDDKDDEINLQCQLVEKLKEQILDQDELLASTRGDSDKVQTELGRLQTESESAKAEVREVLQALEELAVNYDQKSQEVEEKSLHNKQLAEQLSHKMANLMELEAELAQMQEVSSQQRKRIADVLNGLMKDLSEFSSIVGNGELKLPVEISGAIEEEFTVARLYISKIKSEVKSMVKRCRQLENMQLECHRKMEETSRELSSCQLLISQHEAKIRSLTEYMQNVEQKKRQLEDNYDALSEELYTLQNSESHVAELDGGEKADREADGKKAAVRPALHAESRQTQLSRLRDEINEKQRLIDELTDKNQALELELAHVRSSFSNLKLQDDSKSACLEQMSFQQERHEQSKQDLKGLEETVARELQTLHNLRKLFVQDLTTRVKKSSEIGPDDSGGSNTQKQKISFLENNLDQLTKVHKQLVRDNADLRCELPKLEKRLRSTAERVRALETALKDAKQGAMNDRRRYQQEVERIRDAMRLRYPLRRPNAAQIAKPVRPGHHVTATSPTSFSVTRASKPATSYSNARFLQDEKMENSQKTNTVGYSTVRSIDILSSCPLDVENGNSTDINDNRSDVHCGSMVDDASRVYIMQQETAAS", "length": 1033, "header": "tr|A0A0R4IWI7-1|A0A0R4IWI7_DANRE Isoform 1 of Kinesin family member 5Aa OS=Danio rerio OX=7955 GN=kif5aa PE=3 SV=1 CANONICAL=A0A0R4IWI7-1" }, "isoforms": [ { "isoform_ac": "A0A0R4IWI7-1", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7/entry#A0A0R4IWI7-1", "sequence": { "sequence": "MTDAAAECNIKVLCRFRPLNQAEILRGDKFLPTFQGDDTVIIGGKSYAFDRVFPTNTTQEQVYNTCAKQIVKDVLGGYNGTIFAYGQTSSGKTHTMEGNLHDPQQMGIIPRIAEDIFNHIFSMDENLEFHIKVSYFEIYMEKIRDLLDVTKTNLSVHEDKNRVPYVKGCTERFVSSPEEVMDVIDEGKSNRHVAVTNMNEHSSRSHSIFLINIKQEHVETEQKLCGKLYLVDLAGSEKVSKTGAAGAVLDEAKNINKSLSALGNVISALAEGTKSHVPYRDSKMTRILQDSLGGNCRTTMFICCSPSSYNDAETKSTLMFGQRAKTIKNTASINLELTAEQWKRKYEKEKEKNKSLRDSMQRLELELRRWRNGEKVPETEQTDADVVKLDVSEETSLDNEKSCERQRERERDSDTSSIVVRISEEERQKYEEEIRKLYRQLDDKDDEINLQCQLVEKLKEQILDQDELLASTRGDSDKVQTELGRLQTESESAKAEVREVLQALEELAVNYDQKSQEVEEKSLHNKQLAEQLSHKMANLMELEAELAQMQEVSSQQRKRIADVLNGLMKDLSEFSSIVGNGELKLPVEISGAIEEEFTVARLYISKIKSEVKSMVKRCRQLENMQLECHRKMEETSRELSSCQLLISQHEAKIRSLTEYMQNVEQKKRQLEDNYDALSEELYTLQNSESHVAELDGGEKADREADGKKAAVRPALHAESRQTQLSRLRDEINEKQRLIDELTDKNQALELELAHVRSSFSNLKLQDDSKSACLEQMSFQQERHEQSKQDLKGLEETVARELQTLHNLRKLFVQDLTTRVKKSSEIGPDDSGGSNTQKQKISFLENNLDQLTKVHKQLVRDNADLRCELPKLEKRLRSTAERVRALETALKDAKQGAMNDRRRYQQEVERIRDAMRLRYPLRRPNAAQIAKPVRPGHHVTATSPTSFSVTRASKPATSYSNARFLQDEKMENSQKTNTVGYSTVRSIDILSSCPLDVENGNSTDINDNRSDVHCGSMVDDASRVYIMQQETAAS", "length": 1033, "header": "tr|A0A0R4IWI7-1|A0A0R4IWI7_DANRE Isoform 1 of Kinesin family member 5Aa OS=Danio rerio OX=7955 GN=kif5aa PE=3 SV=1 CANONICAL=A0A0R4IWI7-1" }, "locus": {} } ], "glycosylation": [], "phosphorylation": [], "glycation": [], "keywords": [], "publication": [ { "title": "The zebrafish reference genome sequence and its relationship to the human genome.", "journal": "Nature", "date": "2013", "authors": "Howe Kerstin, Clark Matthew D, Torroja Carlos F, Torrance James, Berthelot Camille, Muffato Matthieu, Collins John E, Humphray Sean, McLaren Karen, Matthews Lucy, McLaren Stuart, Sealy Ian, Caccamo Mario, Churcher Carol, Scott Carol, Barrett Jeffrey C, Koch Romke, Rauch Gerd-J\u00f6rg, White Simon, Chow William, Kilian Britt, Quintais Leonor T, Guerra-Assun\u00e7\u00e3o Jos\u00e9 A, Zhou Yi, Gu Yong, Yen Jennifer, Vogel Jan-Hinnerk, Eyre Tina, Redmond Seth, Banerjee Ruby, Chi Jianxiang, Fu Beiyuan, Langley Elizabeth, Maguire Sean F, Laird Gavin K, Lloyd David, Kenyon Emma, Donaldson Sarah, Sehra Harminder, Almeida-King Jeff, Loveland Jane, Trevanion Stephen, Jones Matt, Quail Mike, Willey Dave, Hunt Adrienne, Burton John, Sims Sarah, McLay Kirsten, Plumb Bob, Davis Joy, Clee Chris, Oliver Karen, Clark Richard, Riddle Clare, Elliot David, Eliott David, Threadgold Glen, Harden Glenn, Ware Darren, Begum Sharmin, Mortimore Beverley, Mortimer Beverly, Kerry Giselle, Heath Paul, Phillimore Benjamin, Tracey Alan, Corby Nicole, Dunn Matthew, Johnson Christopher, Wood Jonathan, Clark Susan, Pelan Sarah, Griffiths Guy, Smith Michelle, Glithero Rebecca, Howden Philip, Barker Nicholas, Lloyd Christine, Stevens Christopher, Harley Joanna, Holt Karen, Panagiotidis Georgios, Lovell Jamieson, Beasley Helen, Henderson Carl, Gordon Daria, Auger Katherine, Wright Deborah, Collins Joanna, Raisen Claire, Dyer Lauren, Leung Kenric, Robertson Lauren, Ambridge Kirsty, Leongamornlert Daniel, McGuire Sarah, Gilderthorp Ruth, Griffiths Coline, Manthravadi Deepa, Nichol Sarah, Barker Gary, Whitehead Siobhan, Kay Michael, Brown Jacqueline, Murnane Clare, Gray Emma, Humphries Matthew, Sycamore Neil, Barker Darren, Saunders David, Wallis Justene, Babbage Anne, Hammond Sian, Mashreghi-Mohammadi Maryam, Barr Lucy, Martin Sancha, Wray Paul, Ellington Andrew, Matthews Nicholas, Ellwood Matthew, Woodmansey Rebecca, Clark Graham, Cooper James D, Cooper James, Tromans Anthony, Grafham Darren, Skuce Carl, Pandian Richard, Andrews Robert, Harrison Elliot, Kimberley Andrew, Garnett Jane, Fosker Nigel, Hall Rebekah, Garner Patrick, Kelly Daniel, Bird Christine, Palmer Sophie, Gehring Ines, Berger Andrea, Dooley Christopher M, Ersan-\u00dcr\u00fcn Z\u00fcbeyde, Eser Cigdem, Geiger Horst, Geisler Maria, Karotki Lena, Kirn Anette, Konantz Judith, Konantz Martina, Oberl\u00e4nder Martina, Rudolph-Geiger Silke, Teucke Mathias, Lanz Christa, Raddatz G\u00fcnter, Osoegawa Kazutoyo, Zhu Baoli, Rapp Amanda, Widaa Sara, Langford Cordelia, Yang Fengtang, Schuster Stephan C, Carter Nigel P, Harrow Jennifer, Ning Zemin, Herrero Javier, Searle Steve M J, Enright Anton, Geisler Robert, Plasterk Ronald H A, Lee Charles, Westerfield Monte, de Jong Pieter J, Zon Leonard I, Postlethwait John H, N\u00fcsslein-Volhard Christiane, Hubbard Tim J P, Roest Crollius Hugues, Rogers Jane, Stemple Derek L", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "reference": [ { "type": "PubMed", "id": "23594743", "url": "https://glygen.org/publication/PubMed/23594743" } ] }, { "title": "Temporal and tissue specific gene expression patterns of the zebrafish kinesin-1 heavy chain family, kif5s, during development.", "journal": "Gene Expr. Patterns", "date": "2013", "authors": "Campbell Philip D, Marlow Florence L", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "reference": [ { "type": "PubMed", "id": "23684767", "url": "https://glygen.org/publication/PubMed/23684767" } ] }, { "title": "Highly efficient CRISPR/Cas9-mediated knock-in in zebrafish by homology-independent DNA repair.", "journal": "Genome Res.", "date": "2014", "authors": "Auer Thomas O, Duroure Karine, De Cian Anne, Concordet Jean-Paul, Del Bene Filippo", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "reference": [ { "type": "PubMed", "id": "24179142", "url": "https://glygen.org/publication/PubMed/24179142" } ] }, { "title": "Unique function of Kinesin Kif5A in localization of mitochondria in axons.", "journal": "J. Neurosci.", "date": "2014", "authors": "Campbell Philip D, Shen Kimberle, Sapio Matthew R, Glenn Thomas D, Talbot William S, Marlow Florence L", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" }, { "database": "RefSeq", "id": "NP_001186705", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001186705" } ], "reference": [ { "type": "PubMed", "id": "25355224", "url": "https://glygen.org/publication/PubMed/25355224" } ] }, { "title": "Deletion of a kinesin I motor unmasks a mechanism of homeostatic branching control by neurotrophin-3.", "journal": "Elife", "date": "2015", "authors": "Auer Thomas O, Xiao Tong, Bercier Valerie, Gebhardt Christoph, Duroure Karine, Concordet Jean-Paul, Wyart Claire, Suster Maximiliano, Kawakami Koichi, Wittbrodt Joachim, Baier Herwig, Del Bene Filippo", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" }, { "database": "RefSeq", "id": "NP_001186705", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001186705" } ], "reference": [ { "type": "PubMed", "id": "26076409", "url": "https://glygen.org/publication/PubMed/26076409" } ] }, { "title": "2C-Cas9: a versatile tool for clonal analysis of gene function.", "journal": "Genome Res.", "date": "2016", "authors": "Di Donato Vincenzo, De Santis Flavia, Auer Thomas O, Testa No\u00e9, S\u00e1nchez-Iranzo H\u00e9ctor, Mercader Nadia, Concordet Jean-Paul, Del Bene Filippo", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "reference": [ { "type": "PubMed", "id": "26957310", "url": "https://glygen.org/publication/PubMed/26957310" } ] }, { "title": "Gene evolution and gene expression after whole genome duplication in fish: the PhyloFish database.", "journal": "BMC Genomics", "date": "2016", "authors": "Pasquier Jeremy, Cabau C\u00e9dric, Nguyen Thaovi, Jouanno Elodie, Severac Dany, Braasch Ingo, Journot Laurent, Pontarotti Pierre, Klopp Christophe, Postlethwait John H, Guiguen Yann, Bobe Julien", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "reference": [ { "type": "PubMed", "id": "27189481", "url": "https://glygen.org/publication/PubMed/27189481" } ] }, { "title": "MicroRNA miR-29 controls a compensatory response to limit neuronal iron accumulation during adult life and aging.", "journal": "BMC Biol.", "date": "2017", "authors": "Ripa Roberto, Dolfi Luca, Terrigno Marco, Pandolfini Luca, Savino Aurora, Arcucci Valeria, Groth Marco, Terzibasi Tozzini Eva, Baumgart Mario, Cellerino Alessandro", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "reference": [ { "type": "PubMed", "id": "28193224", "url": "https://glygen.org/publication/PubMed/28193224" } ] }, { "title": "In Vivo Fast Nonlinear Microscopy Reveals Impairment of Fast Axonal Transport Induced by Molecular Motor Imbalances in the Brain of Zebrafish Larvae.", "journal": "ACS Nano", "date": "2022", "authors": "Grimaud Baptiste, Fr\u00e9taud Maxence, Terras Feriel, B\u00e9nassy Antoine, Duroure Karine, Bercier Val\u00e9rie, Tripp\u00e9-Allard Ga\u00eblle, Mohammedi Rabei, Gacoin Thierry, Del Bene Filippo, Marquier Fran\u00e7ois, Langevin Christelle, Treussart Fran\u00e7ois", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "reference": [ { "type": "PubMed", "id": "36459488", "url": "https://glygen.org/publication/PubMed/36459488" } ] } ], "pathway": [ { "id": "dre:566086", "name": "", "url": "https://www.genome.jp/dbget-bin/www_bget?dre:566086", "resource": "KEGG Pathway" } ], "orthologs": [ { "uniprot_canonical_ac": "A0A8M3ATT8-1", "protein_name": "Kinesin heavy chain isoform X1", "gene_name": "kif5ab", "tax_id": 7955, "organism": "Danio rerio", "sequence": { "sequence": "MADISAECNIRVLCRFRPLNQSEILRGDKFMPTFQGDDTVIIAGRSYVFDKVFPTNCTQEQVYNTCAQQIVKDVLDGYNGTIFAYGQTSSGKTYTMEGKLHDANGRGIIPRIAEDIFNHIYTMDENLEFHIKVSYFEIYMDKIRDLLDVTKTNLSVHEDKNRVPYVKGCTERFVSSPEEVMDLIDEGKANRHVAVTNMNEHSSRSHSIFLINIKQEHVETEQKLCGKLYLVDLAGSEKVSKTGAEGAVLDEAKNINKSLSALGNVISALAEGTKTHVPYRDSKMTRILQDSLGGNCRTTMFICCSPSAYNDAETKSTLMFGQRAKTIMNSASVNLELTAEQWKRKYEKEKEKNKDLKESMQRLEAELNHWRNGESVVLITPVSPAECDVTEDTAVDNQSHGQTELIPEQHNSRYEEEIQQLYRQLDDKDDEINLQCQLVEKLKEQMLDQEELLACARADLERVQCDVRRLQADSESSKLEVQEVLQALEELALSYDHKSLEAQDNSRHNRRLTEELAHTTSALLSLESDFSRLQEVNGQQRKRITEVLNTLVKDLNDFSFILGNGDLRLPSELSGVLEEEYAVVCVYMSKVKSELKTLVKRCRQLESLQTDCHRKMEETGRELSSCQLLISQHEAKIRSLTEYMQNMELKKRQLEENYDCLSEELAKLQNTESILDRPLDTDESVNVKSHKAVDQKSEVQREPQHKQLGRLRDDINHKQKIIDELTDDNQRLDLQLEQLSVEFSVLKSREHEKSRQLEELRYLHERQEQTRQDMKGLEETVVSAYRKYDISNDNNNGVYDRPAHFSLKARELQTLHNLRKLFVQDLTARVKRSSELDPDDSSGCSTQKQKISFLENNLDQLTKVHKQLVRDNADLRCELPKLEKRLRSTAERVRALEEALREAKEGAMKDRRRYQQEVERIKDVMRSRNPFRRPQAALIAKPIRPGHYPASLSANHMFLRSRDQPITFSNAMFNSSSEKQKLTSSKTESSLTSRTLSEHERQTHETTNCTQKLHITNGNSSDVNDNSECRSSTITDEPQQKHHQEQPVAS", "length": 1050 }, "evidence": [ { "id": "MGI:109564", "url": "https://alliancegenome.org/gene/MGI:109564#orthology", "database": "AGR" }, { "id": "HGNC:6323", "url": "https://alliancegenome.org/gene/HGNC:6323#orthology", "database": "AGR" } ], "glygen_name": "Zebrafish", "common_name": "Zebrafish" }, { "uniprot_canonical_ac": "P17210-1", "protein_name": "Kinesin heavy chain", "gene_name": "Khc", "tax_id": 7227, "organism": "Drosophila melanogaster", "sequence": { "sequence": "MSAEREIPAEDSIKVVCRFRPLNDSEEKAGSKFVVKFPNNVEENCISIAGKVYLFDKVFKPNASQEKVYNEAAKSIVTDVLAGYNGTIFAYGQTSSGKTHTMEGVIGDSVKQGIIPRIVNDIFNHIYAMEVNLEFHIKVSYYEIYMDKIRDLLDVSKVNLSVHEDKNRVPYVKGATERFVSSPEDVFEVIEEGKSNRHIAVTNMNEHSSRSHSVFLINVKQENLENQKKLSGKLYLVDLAGSEKVSKTGAEGTVLDEAKNINKSLSALGNVISALADGNKTHIPYRDSKLTRILQESLGGNARTTIVICCSPASFNESETKSTLDFGRRAKTVKNVVCVNEELTAEEWKRRYEKEKEKNARLKGKVEKLEIELARWRAGETVKAEEQINMEDLMEASTPNLEVEAAQTAAAEAALAAQRTALANMSASVAVNEQARLATECERLYQQLDDKDEEINQQSQYAEQLKEQVMEQEELIANARREYETLQSEMARIQQENESAKEEVKEVLQALEELAVNYDQKSQEIDNKNKDIDALNEELQQKQSVFNAASTELQQLKDMSSHQKKRITEMLTNLLRDLGEVGQAIAPGESSIDLKMSALAGTDASKVEEDFTMARLFISKMKTEAKNIAQRCSNMETQQADSNKKISEYEKDLGEYRLLISQHEARMKSLQESMREAENKKRTLEEQIDSLREECAKLKAAEHVSAVNAEEKQRAEELRSMFDSQMDELREAHTRQVSELRDEIAAKQHEMDEMKDVHQKLLLAHQQMTADYEKVRQEDAEKSSELQNIILTNERREQARKDLKGLEDTVAKELQTLHNLRKLFVQDLQQRIRKNVVNEESEEDGGSLAQKQKISFLENNLDQLTKVHKQLVRDNADLRCELPKLEKRLRCTMERVKALETALKEAKEGAMRDRKRYQYEVDRIKEAVRQKHLGRRGPQAQIAKPIRSGQGAIAIRGGGAVGGPSPLAQVNPVNS", "length": 975 }, "evidence": [ { "id": "MGI:109564", "url": "https://alliancegenome.org/gene/MGI:109564#orthology", "database": "AGR" }, { "id": "HGNC:6323", "url": "https://alliancegenome.org/gene/HGNC:6323#orthology", "database": "AGR" } ], "glygen_name": "Fruit fly", "common_name": "Fruit fly" }, { "uniprot_canonical_ac": "P33175-1", "protein_name": "Kinesin heavy chain isoform 5A", "gene_name": "Kif5a", "tax_id": 10090, "organism": "Mus musculus", "sequence": { "sequence": "MAETNNECSIKVLCRFRPLNQAEILRGDKFIPIFQGDDSVIIGGKPYVFDRVFPPNTTQEQVYHACAMQIVKDVLAGYNGTIFAYGQTSSGKTHTMEGKLHDPQLMGIIPRIARDIFNHIYSMDENLEFHIKVSYFEIYLDKIRDLLDVTKTNLSVHEDKNRVPFVKGCTERFVSSPEEILDVIDEGKSNRHVAVTNMNEHSSRSHSIFLINIKQENVETEQKLSGKLYLVDLAGSEKVSKTGAEGAVLDEAKNINKSLSALGNVISALAEGTKSYVPYRDSKMTRILQDSLGGNCRTTMFICCSPSSYNDAETKSTLMFGQRAKTIKNTASVNLELTAEQWKKKYEKEKEKTKAQKETIAKLEAELSRWRNGENVPETERLAGEDSALGAELCEETPVNDNSSIVVRIAPEERQKYEEEIRRLYKQLDDKDDEINQQSQLIEKLKQQMLDQEELLVSTRGDNEKVQRELSHLQSENDAAKDEVKEVLQALEELAVNYDQKSQEVEEKSQQNQLLVDELSQKVATMLSLESELQRLQEVSGHQRKRIAEVLNGLMRDLSEFSVIVGNGEIKLPVEISGAIEEEFTVARLYISKIKSEVKSVVKRCRQLENLQVECHRKMEVTGRELSSCQLLISQHEAKIRSLTEYMQTVELKKRHLEESYDSLSDELARLQAHETVHEVALKDKEPDTQDAEEVKKALELQMENHREAHHRQLARLRDEINEKQKTIDELKDLNQKLQLELEKLQADYERLKNEENEKSAKLQELTFLYERHEQSKQDLKGLEETVARELQTLHNLRKLFVQDVTTRVKKSAEMEPEDSGGIHSQKQKISFLENNLEQLTKVHKQLVRDNADLRCELPKLEKRLRATAERVKALEGALKEAKEGAMKDKRRYQQEVDRIKEAVRYKSSGKRGHSAQIAKPVRPGHYPASSPTNPYGTRSPECISYTNNLFQNYQNLHLQAAPSSTSDMYFASSGATSVAPLASYQKANMDNGNATDINDNRSDLPCGYEAEDQAKLFPLHQETAAS", "length": 1027 }, "evidence": [ { "id": "ZFIN:ZDB-GENE-070912-141", "url": "https://alliancegenome.org/gene/ZFIN:ZDB-GENE-070912-141#orthology", "database": "AGR" }, { "id": "MGI:109564", "url": "https://alliancegenome.org/gene/MGI:109564#orthology", "database": "AGR" }, { "id": "HGNC:6323", "url": "https://alliancegenome.org/gene/HGNC:6323#orthology", "database": "AGR" } ], "glygen_name": "Mouse", "common_name": "Mouse" }, { "uniprot_canonical_ac": "Q12840-1", "protein_name": "Kinesin heavy chain isoform 5A", "gene_name": "KIF5A", "tax_id": 9606, "organism": "Homo sapiens", "sequence": { "sequence": "MAETNNECSIKVLCRFRPLNQAEILRGDKFIPIFQGDDSVVIGGKPYVFDRVFPPNTTQEQVYHACAMQIVKDVLAGYNGTIFAYGQTSSGKTHTMEGKLHDPQLMGIIPRIARDIFNHIYSMDENLEFHIKVSYFEIYLDKIRDLLDVTKTNLSVHEDKNRVPFVKGCTERFVSSPEEILDVIDEGKSNRHVAVTNMNEHSSRSHSIFLINIKQENMETEQKLSGKLYLVDLAGSEKVSKTGAEGAVLDEAKNINKSLSALGNVISALAEGTKSYVPYRDSKMTRILQDSLGGNCRTTMFICCSPSSYNDAETKSTLMFGQRAKTIKNTASVNLELTAEQWKKKYEKEKEKTKAQKETIAKLEAELSRWRNGENVPETERLAGEEAALGAELCEETPVNDNSSIVVRIAPEERQKYEEEIRRLYKQLDDKDDEINQQSQLIEKLKQQMLDQEELLVSTRGDNEKVQRELSHLQSENDAAKDEVKEVLQALEELAVNYDQKSQEVEEKSQQNQLLVDELSQKVATMLSLESELQRLQEVSGHQRKRIAEVLNGLMKDLSEFSVIVGNGEIKLPVEISGAIEEEFTVARLYISKIKSEVKSVVKRCRQLENLQVECHRKMEVTGRELSSCQLLISQHEAKIRSLTEYMQSVELKKRHLEESYDSLSDELAKLQAQETVHEVALKDKEPDTQDADEVKKALELQMESHREAHHRQLARLRDEINEKQKTIDELKDLNQKLQLELEKLQADYEKLKSEEHEKSTKLQELTFLYERHEQSKQDLKGLEETVARELQTLHNLRKLFVQDVTTRVKKSAEMEPEDSGGIHSQKQKISFLENNLEQLTKVHKQLVRDNADLRCELPKLEKRLRATAERVKALEGALKEAKEGAMKDKRRYQQEVDRIKEAVRYKSSGKRGHSAQIAKPVRPGHYPASSPTNPYGTRSPECISYTNSLFQNYQNLYLQATPSSTSDMYFANSCTSSGATSSGGPLASYQKANMDNGNATDINDNRSDLPCGYEAEDQAKLFPLHQETAAS", "length": 1032 }, "evidence": [ { "id": "ZFIN:ZDB-GENE-070912-141", "url": "https://alliancegenome.org/gene/ZFIN:ZDB-GENE-070912-141#orthology", "database": "AGR" }, { "id": "MGI:109564", "url": "https://alliancegenome.org/gene/MGI:109564#orthology", "database": "AGR" }, { "id": "HGNC:6323", "url": "https://alliancegenome.org/gene/HGNC:6323#orthology", "database": "AGR" } ], "glygen_name": "Human", "common_name": "Human" }, { "uniprot_canonical_ac": "Q6QLM7-1", "protein_name": "Kinesin heavy chain isoform 5A", "gene_name": "Kif5a", "tax_id": 10116, "organism": "Rattus norvegicus", "sequence": { "sequence": "MAETNNECSIKVLCRFRPLNQAEILRGDKFIPIFQGDDSVIIGGKPYVFDRVFPPNTTQEQVYHACAMQIVKDVLAGYNGTIFAYGQTSSGKTHTMEGKLHDPQLMGIIPRIARDIFNHIYSMDENLEFHIKVSYFEIYLDKIRDLLDVTKTNLSVHEDKNRVPFVRGCTERFVSSPEEILDVIDEGKSNRHVAVTNMNEHSSRSHSIFLINIKQENIETEQKLSGKLYLADLAGSEKVSKTGAEGAVLDEAKNINKSLSALGNVISALAEGTKSYVPYRDSKMTRILQDSLGGNCRTTMFICCSPSSYNDAETKSTLMFGQRAKTIKNTASVNLELTAEQWKKKYEKEKEKTKAQKETIAKLEAELSRWRNGENVPETERLAGEDSALAAEICEETPVNDNSSIVVRIAPEERQKYEEEIRRLYKQLDDKDDEINQQSQLIEKLKQQMLDQEELLVSTRGDNEKVQRELSHLQSENDAAKEEVKEVLQALEELAVNYDQKSQEVEEKSQQNQLLVDELSQKVATMLSLESEPQRLQEVSGHQRKRIAEVLNGLMKDLSEFSVIVGNGEIKLPVEISGAIEEEFTVARLYISKIKSEVKSVVKRCRQLENLQVECHRKMEVTGRELSSCQLLISQHEAKIRSLTEYMQTVELKKRHLEESYDSLSDELAKLQAQETVHEVALKDKEPDTQDAEEVKKALELQMENHREAHHRQLARLRDEINEKQKTIDELKDLDQKLQLELEKLQADYERLKNEENEKSAKLQELTFLYERHEQSKQDLKGLEETVARELQTLHNLRKLFVQDVTTRVKKSAEMEPEDSGGIHSQKQKISFLENNLEQLTEVHKQLVRDNADLRCELPKLEKRLRATAERVKALEGALKEAKEGAMKDKRRYQQEVDRIKEAVRYKSSGKRGHSAQIAKPVRPGHYPASSPTNPYGTRSPECISYTNNLFQNYQNLHLQAAPSSTSDVYFASNGATSVAPLASYQKANTDNGNATDINDNRSDLPCGYEAEDPAKLFPLHQETAAS", "length": 1027 }, "evidence": [ { "id": "MGI:109564", "url": "https://alliancegenome.org/gene/MGI:109564#orthology", "database": "AGR" }, { "id": "HGNC:6323", "url": "https://alliancegenome.org/gene/HGNC:6323#orthology", "database": "AGR" } ], "glygen_name": "Rat", "common_name": "Rat" } ], "go_annotation": { "categories": [ { "name": "Molecular Function", "total": 4, "go_terms": [ { "name": "ATP binding", "id": "GO:0005524", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" }, { "name": "microtubule binding", "id": "GO:0008017", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008017", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" }, { "name": "ATP hydrolysis activity", "id": "GO:0016887", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016887", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" }, { "name": "plus-end-directed microtubule motor activity", "id": "GO:0008574", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008574", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" } ] }, { "name": "Cellular Component", "total": 5, "go_terms": [ { "name": "cytoplasm", "id": "GO:0005737", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" }, { "name": "microtubule", "id": "GO:0005874", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005874", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" }, { "name": "kinesin complex", "id": "GO:0005871", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005871", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" }, { "name": "dendrite cytoplasm", "id": "GO:0032839", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032839", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" }, { "name": "axon cytoplasm", "id": "GO:1904115", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1904115", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" } ] }, { "name": "Biological Process", "total": 5, "go_terms": [ { "name": "neuron projection maintenance", "id": "GO:1990535", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990535", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" }, { "name": "axon guidance", "id": "GO:0007411", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007411", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" }, { "name": "anterograde dendritic transport of neurotransmitter receptor complex", "id": "GO:0098971", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098971", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" }, { "name": "synaptic vesicle transport", "id": "GO:0048489", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048489", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" }, { "name": "axonal transport of mitochondrion", "id": "GO:0019896", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019896", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IWI7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IWI7" } ], "pmid": "" } ] } ] }, "pro_annotation": [], "site_annotation": [ { "start_pos": 1000, "end_pos": 1002, "annotation": "n_glycosylation_sequon" }, { "start_pos": 1007, "end_pos": 1009, "annotation": "n_glycosylation_sequon" }, { "start_pos": 153, "end_pos": 155, "annotation": "n_glycosylation_sequon" }, { "start_pos": 256, "end_pos": 258, "annotation": "n_glycosylation_sequon" }, { "start_pos": 353, "end_pos": 355, "annotation": "n_glycosylation_sequon" }, { "start_pos": 56, "end_pos": 58, "annotation": "n_glycosylation_sequon" }, { "start_pos": 79, "end_pos": 81, "annotation": "n_glycosylation_sequon" } ], "ptm_annotation": [], "interactions": [], "reactions": [], "reaction_participants": [], "reaction_enzymes": [], "biomarkers": [], "structures": [], "synthesized_glycans": [], "enzyme_annotation": [], "cluster_types": [ { "name": "homologset.agr", "label": "AGR Homologs" } ], "sequence_features": { "n_linked_sites": [], "o_linked_sites": [], "snv_sites": [], "glycation_sites": [], "phosphorylation_sites": [], "sequon_annotation_sites": [ { "start_pos": 1000, "end_pos": 1002 }, { "start_pos": 1007, "end_pos": 1009 }, { "start_pos": 153, "end_pos": 155 }, { "start_pos": 256, "end_pos": 258 }, { "start_pos": 353, "end_pos": 355 }, { "start_pos": 56, "end_pos": 58 }, { "start_pos": 79, "end_pos": 81 } ] }, "section_stats": [ { "table_id": "glycosylation", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 }, { "field": "total", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_reported", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 }, { "field": "total", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_reported_with_glycan", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 }, { "field": "total", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_predicted", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 }, { "field": "total", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_automatic_literature_mining", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 }, { "field": "total", "count": 0 } ], "sort_fields": [] }, { "table_id": "phosphorylation", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "snv", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "snv_disease", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "snv_non_disease", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "publication", "table_stats": [ { "field": "total", "count": 9 } ], "sort_fields": [ "title", "journal", "date", "authors" ] } ] }