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Protein Coding Gene : Nisch nischarin

Primary Identifier  MGI:1928323 Organism  mouse, laboratory
Chromosome  14 NCBI Gene Number  64652
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables integrin binding activity. Acts upstream of or within Rac protein signal transduction; actin cytoskeleton organization; and negative regulation of cell migration. Located in cytosol. Is expressed in several structures, including alimentary system; brain; cardiovascular system; genitourinary system; and integumental system. Used to study otitis media. Human ortholog(s) of this gene implicated in congestive heart failure. Orthologous to human NISCH (nischarin).
PHENOTYPE: Mice homozygous for either a knock-out or hypomorphic allele exhibit hearing loss associated with increased susceptibility to otitis media. [provided by MGI curators]
  • synonyms:
  • MGI:3653500,
  • 1200007D05Rik,
  • AW494485,
  • Nisch,
  • MGI:1921365,
  • RIKEN cDNA 3202002H23 gene,
  • nischarin,
  • 3202002H23Rik,
  • expressed sequence AW494485,
  • edsn,
  • MGI:2145818,
  • edison,
  • RIKEN cDNA 1200007D05 gene,
  • MGI:1924216

Features --> Cross References

Genome

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0 CDSs

0 Exons

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0 Involved In Mutations

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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

7 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

 

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