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Protein Coding Gene : Anp32b acidic nuclear phosphoprotein 32 family member B

Primary Identifier  MGI:1914878 Organism  mouse, laboratory
Chromosome  4 NCBI Gene Number  67628
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable RNA polymerase binding activity and histone binding activity. Acts upstream of or within several processes, including inner ear development; roof of mouth development; and ventricular system development. Located in nucleus. Is expressed in several structures, including cerebral cortex ventricular layer; eye; heart; metanephros; and upper jaw. Orthologous to human ANP32B (acidic nuclear phosphoprotein 32 family member B).
PHENOTYPE: Mice homozygous for a knock-out allele exhibit background-sensitive partial perinatal lethality with failure to initiate breathing, craniofacial defects, enlarged brain ventricle, expanded inner ear cavities, plate closure defects, decreased body weight, premature aging, and premature death. [provided by MGI curators]
  • synonyms:
  • acidic nuclear phosphoprotein 32 family member B,
  • PAL31,
  • RIKEN cDNA 2410015B15 gene,
  • 2410015B15Rik,
  • MGI:1926203,
  • PHAPI2a,
  • Anp32b

Features --> Cross References

Genome

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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

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Expression

Gene --> Expression annotations

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Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

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