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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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