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Gene : ATXN10 Homo sapiens

Name  ? ataxin 10 Cytological Location  22q13.31
Brief Description  ataxin 10
Description  This gene encodes a protein that may function in neuron survival, neuron differentiation, and neuritogenesis. These roles may be carried out via activation of the mitogen-activated protein kinase cascade. Expansion of an ATTCT repeat from 9-32 copies to 800-4500 copies in an intronic region of this locus has been associated with spinocerebellar ataxia, type 10. Alternatively spliced transcript variants have been described.[provided by RefSeq, Jul 2016]
  • synonyms:
  • HGNC:10549,
  • OTTHUMG00000150451,
  • SCA10,
  • NM_013236,
  • AK095309,
  • E46L,
  • FLJ37990,
  • ATXN10,
  • spinocerebellar ataxia 10,
  • E46L,
  • uc003bgm.3,
  • SCA10
  • identifiers:
  • 25814,
  • ENSG00000130638,
  • ATXN10

Genome feature

Region: gene ? Length: 173474  
Location: 22:45671834-45845307 Cyto location: 22q13.31

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

3740 SNPs

5 Cross References

19 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results