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Protein Coding Gene : Anp32e acidic nuclear phosphoprotein 32 family member E

Primary Identifier  MGI:1913721 Organism  mouse, laboratory
Chromosome  3 NCBI Gene Number  66471
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables phosphatase inhibitor activity. Predicted to be involved in regulation of apoptotic process. Located in cytoplasmic vesicle and nucleus. Is active in cytoplasmic vesicle membrane; glutamatergic synapse; and postsynaptic density membrane. Is expressed in brain; liver; retina layer; and skeletal muscle. Orthologous to human ANP32E (acidic nuclear phosphoprotein 32 family member E).
PHENOTYPE: Mice homozygous for a gene trapped allele exhibit mild neurological deficits. Mice homozygous for a knock-out allele are phenotypically normal. [provided by MGI curators]
  • synonyms:
  • AI047746,
  • expressed sequence AI326868,
  • expressed sequence AI047746,
  • LANP-L,
  • CPD1,
  • MGC:11640,
  • MGI:2139684,
  • RIKEN cDNA 2810018A15 gene,
  • AI326868,
  • Anp32e,
  • 2810018A15Rik,
  • MGI:2139621,
  • acidic nuclear phosphoprotein 32 family member E

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

0 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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0 Driver For