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Heritable Phenotypic Marker : elap eye lens aplasia
Primary Identifier  MGI:105916 Organism  mouse, laboratory
Chromosome  2 Mgi Type  heritable phenotypic marker
description  PHENOTYPE: Homozygotes for a spontaneous mutation exhibit eye defects including microphthalmia, aphakia, absence of the anterior chamber, dystrophy of the cornea and vitreous body, and retinal disorganization. [provided by MGI curators]
  • synonyms:
  • lens aplasia,
  • MGD-MRK-33296,
  • elap,
  • lap,
  • MGD-MRK-33593,
  • eye lens aplasia
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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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0 Driver For





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