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Cm
Gene Detail
 Symbol
Name
ID
Cm
coloboma deletion region
MGI:88424
Feature Type heritable phenotypic marker
Genetic Map
Chromosome 2
Syntenic

Mapping data(5)
Alleles
and
phenotypes
All alleles(1) : Radiation induced(1)
 
Homozygous animals die in utero. Heterozygous mutants exhibit abnormal posture, abnormal head movements, hyperactivity, microphthalmia, and abnormalities of the pigmented choroid.
 
Human Diseases Modeled Using Mouse Cm (1)    Alleles Annotated to Human Diseases(1)    Phenotype Images(1)
Other database
links
Entrez Gene111346
References (Earliest) J:13450 Searle AG, Brachyrrhine, Br. Mouse News Lett. 1966;35:27
(Latest) J:198682 Leo D, et al., Transgenic mouse models for ADHD. Cell Tissue Res. 2013 May 17;
All references(27)
Other
accession IDs
MGD-MRK-2023

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory