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 Gene

111346

References

(Earliest) J:13450 Searle AG, Brachyrrhine, Br. Mouse News Lett. 1966;35:27
(Latest) J:185694 Gunn RK, et al., Analysis of sensory, motor and cognitive functions of the coloboma (C3Sn.Cg-Cm/J) mutant mouse. Genes Brain Behav. 2011 Jul;10(5):579-88
All references(26)

Other accession IDs

MGD-MRK-2023