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Heritable Phenotypic Marker : Cm coloboma deletion region
Primary Identifier  MGI:88424 Organism  mouse, laboratory
Chromosome  2 Mgi Type  heritable phenotypic marker
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Used to study attention deficit hyperactivity disorder.
PHENOTYPE: Homozygous animals die in utero. Heterozygous mutants exhibit abnormal posture, abnormal head movements, hyperactivity, microphthalmia, and abnormalities of the pigmented choroid. [provided by MGI curators]
  • synonyms:
  • Cm,
  • coloboma deletion region,
  • MGD-MRK-2023
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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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