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| Nomenclature |
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Symbol:
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Smchd1MommeD1
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Name:
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SMC hinge domain containing 1;
modifiers of murine metastable epiallele D1
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MGI ID: |
MGI:3586547 |
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Gene:
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Smchd1
Location:
Chr17:71344489-71475343 bp, - strand
Genetic Position: Chr17,
41.87 cM
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Mutation
origin |
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Mutation
description |
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Allele
Type: | |
Chemically induced (ENU) |
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Mutation: | |
Single point mutation |
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Mutation details: Mice carrying Tg(Hba1-Gfp)1Ew were treated with ENU. A cytosine to thymine transition in exon 23 results in a nonsense codon. (J:142334)
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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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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Smchd1 Mutation:
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45 strains or lines available |
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| References |
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Original: |
J:99816
Blewitt ME et al.,
"An N-ethyl-N-nitrosourea screen for genes involved in variegation in the mouse."
Proc Natl Acad Sci U S A 2005 May 24;102(21):7629-34
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All: |
3 reference(s)
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Analysis Tools
