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SCAR2 spinocerebellar ataxia, autosomal recessive 2 [ Homo sapiens (human) ]

Gene ID: 1165, discontinued on 25-Jul-2017

Summary

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Official Symbol
SCAR2provided by HGNC
Official Full Name
spinocerebellar ataxia, autosomal recessive 2provided by HGNC
Primary source
HGNC:HGNC:2002
See related
MIM:213200
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
CLA1; CPD3

Genomic context

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Location:
9q34.3

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
spinocerebellar ataxia, autosomal recessive 2
GeneReviews: Not available

General gene information

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Other Names

  • Cerebellar ataxia-1
  • cerebellar ataxia 1 (autosomal recessive)

Property

  • phenotype only

Gene LinkOut

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