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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 8.0.0)

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:
  • MGI:1096568,
  • Atxn10,
  • spinocerebellar ataxia 10 homolog (human),
  • MGI:2145984,
  • TEG-169,
  • testis expressed gene 169,
  • C77170,
  • Tex169,
  • AI325283,
  • expressed sequence C77170,
  • MGI:2146273,
  • ataxin 10,
  • E46,
  • Sca10,
  • expressed sequence AI325283
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Features --> Cross References

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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

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Mouse features --> Functions (GO terms)

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Gene --> Protein-Protein Interactions

Expression

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Genes/Features --> Phenotypes (MP terms)

Disease

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