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Heritable Phenotypic Marker : Cat4 dominant cataract 4
Primary Identifier  MGI:88040 Organism  mouse, laboratory
Chromosome  8 Mgi Type  heritable phenotypic marker
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Used to study cataract.
PHENOTYPE: Homozygotes and heterozygous mutants display eye defects with some or all of: anterior lens opacity with polar adhesions, corneal opacity, anscoria, iris dysplasia, and microphthalmia. For some alleles, homozygotes show anophthalmia or embryonic lethality. [provided by MGI curators]
  • synonyms:
  • Anc,
  • MGD-MRK-1318,
  • Apyc,
  • MGD-MRK-1349,
  • Apcat1,
  • MGD-MRK-1350,
  • Cat4,
  • dominant cataract 4,
  • Pcs-2,
  • Apcat-1,
  • anterior polar cataract,
  • anterior pyramidal cataract,
  • MGD-MRK-13189,
  • polar cataract and small eye 2,
  • MGD-MRK-1383,
  • MGD-MRK-1348,
  • Apc-1,
  • anterior polar cataract 1,
  • anisocoria (radiation induced eye mutation)
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Features --> Cross References

Genome

Sequence Feature Displayer

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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

 

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