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    CPAT1 cerebral palsy, ataxic 1 [ Homo sapiens (human) ]

    Gene ID: 60502, updated on 31-Aug-2024

    Summary

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    Official Symbol
    CPAT1provided by HGNC
    Official Full Name
    cerebral palsy, ataxic 1provided by HGNC
    Primary source
    MIM:605388
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    ACP

    Genomic context

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    Location:
    9p12-q12

    Bibliography

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    Related articles in PubMed

    1. A gene for ataxic cerebral palsy maps to chromosome 9p12-q12. McHale DP, et al. Eur J Hum Genet, 2000 Apr. PMID 10854109

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Associated conditions

    Description Tests
    cerebral palsy, ataxic 1
    OMIM: 605388GeneReviews: Not available

    General gene information

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    Markers

    Property

    • phenotype only

    Gene LinkOut

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