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Protein Coding Gene : Chp1 calcineurin-like EF hand protein 1

Primary Identifier  MGI:1927185 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  56398
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables sodium:proton antiporter activity. Predicted to be involved in several processes, including microtubule cytoskeleton organization; regulation of establishment of protein localization; and regulation of protein modification process. Part of transporter complex. Is active in membrane raft. Is expressed in genitourinary system. Human ortholog(s) of this gene implicated in spastic ataxia. Orthologous to human CHP1 (calcineurin like EF-hand protein 1).
PHENOTYPE: Mice homozygous for an ENU mutation display ataxia and progressive Purkinje cell axonal dystrophy. [provided by MGI curators]
  • synonyms:
  • MGI:2146369,
  • MGI:2146375,
  • Sid470p,
  • AI046351,
  • AA960066,
  • vacillator,
  • expressed sequence AA960066,
  • calcineurin-like EF hand protein 1,
  • MGI:5438383,
  • MGI:1915310,
  • expressed sequence AI046351,
  • 1500003O03Rik,
  • RIKEN cDNA 1500003O03 gene,
  • vac,
  • Chp1

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 Involved In Mutations

0 Strain

0 Transcripts

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

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

5 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For