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Heritable Phenotypic Marker : Mp micropinna microphthalmia
Primary Identifier  MGI:97070 Organism  mouse, laboratory
Chromosome  18 Mgi Type  heritable phenotypic marker
description  PHENOTYPE: Homozygotes for a radiation-induced allele show reduced body weight, closed eyelids, microphthalmia, ciliary body malformation, severe ocular defects, small ears, hindlimb syndactyly and fused phalanges. Heterozygotes show reduced body weight, small earsand similar eye defects but no syndactyly. [provided by MGI curators]
  • synonyms:
  • micropinna microphthalmia,
  • MGD-MRK-12399,
  • Mp
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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





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