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CLA3 cerebellar ataxia 3 (cerebellar parenchyma disorder 1) [ Homo sapiens (human) ]

Gene ID: 1167, updated on 2-Oct-2019

Summary

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Gene symbol
CLA3
Gene description
cerebellar ataxia 3 (cerebellar parenchyma disorder 1)
Primary source
MIM:608029
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
CPD1; SCAR6

Genomic context

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Location:
20q11-q13

Bibliography

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Related articles in PubMed

  1. Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13. Tranebjaerg L, et al. Hum Genet, 2003 Aug. PMID 12811539

GeneRIFs: Gene References Into Functions

Phenotypes

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cerebellar ataxia 3 (cerebellar parenchyma disorder 1)

General gene information

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Markers

Other Names

  • cerebellar ataxia, infantile nonprogressive, autosomal recessive
  • cerebellar parenchyma disorder 1

Property

  • phenotype only

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