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Heritable Phenotypic Marker : Apo anterior polar opacity

Primary Identifier  MGI:88048 Organism  mouse, laboratory
Chromosome  UN Mgi Type  heritable phenotypic marker
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Used to study cataract.
PHENOTYPE: Homozygous mutation of this gene is embryonic lethal. Heterozygous mutants are hyperactive, display circling behavior, cataracts, and some degree of reduced viability as the frequency of heterozygotes is less than the expected Mendelian ratio. [provided by MGI curators]
  • synonyms:
  • MGD-MRK-1363,
  • Apo,
  • anterior polar opacity

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Involved In Mutations

0 Transgenic Expressors

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

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