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Protein Coding Gene : Atxn10 ataxin 10
Primary Identifier  MGI:1859293 Organism  mouse, laboratory
Chromosome  15 NCBI Gene Number  54138
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable enzyme binding activity and identical protein binding activity. Acts upstream of or within cilium assembly. Located in centriole and ciliary basal body. Is expressed in several structures, including central nervous system; metanephros; and retina. Human ortholog(s) of this gene implicated in spinocerebellar ataxia type 10. Orthologous to human ATXN10 (ataxin 10).
PHENOTYPE: Homozygous null mice die at early postimplantation stages. [provided by MGI curators]
  • synonyms:
  • expressed sequence C77170,
  • spinocerebellar ataxia 10 homolog (human),
  • MGI:2146273,
  • Atxn10,
  • Tex169,
  • MGI:2145984,
  • AI325283,
  • E46,
  • C77170,
  • expressed sequence AI325283,
  • testis expressed gene 169,
  • TEG-169,
  • ataxin 10,
  • Sca10,
  • MGI:1096568
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Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

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3 Involved In Mutations

Trail: ProteinCodingGene

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0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

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Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

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Gene --> Protein-Protein Interactions

Expression

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Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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