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| Nomenclature |
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Symbol:
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Cm
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Name:
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coloboma deletion region;
coloboma
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MGI ID: |
MGI:1861106 |
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Gene:
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Cm
Location:
unknown
Genetic Position: Chr2,
Syntenic
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Inner ear defects in Cm/+ mice
Show the 1 image(s) involving this allele.
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Mutation
origin |
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Strain of Origin:
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(C3H/HeH x 101/H)F1
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Mutation
description |
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Allele
Type: | |
Radiation induced |
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Mutation: | |
Intergenic deletion |
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Mutation details: The deletion map of the Cm locus includes Snap25, Plcb, and some or all of Jag1, and numerous other DNA markers. (J:18309, J:54907)
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Inheritance: | |
Semidominant |
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Notes |
This allele represents a deletion including Snap25, Plcb1
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| References |
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Analysis Tools
