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| Nomenclature |
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Symbol:
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Trpv3Nh
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Name:
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transient receptor potential cation channel, subfamily V, member 3;
non-hair
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MGI ID: |
MGI:2384170 |
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Gene:
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Trpv3
Location:
Chr11:73267388-73300363 bp, + strand
Genetic Position: Chr11,
45.25 cM
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Mutation
origin |
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Mutation
description |
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Allele
Type: | |
Spontaneous |
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Mutation: | |
Single point mutation |
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Mutation details: A phenotypic mutant associated with severe dermititis identified in a colony of DS mice. A G1717A point mutation in this allele results in Glycine 573 being replaced with Serine. (J:116026)
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Inheritance: | |
Dominant |
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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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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Trpv3 Mutation:
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5 strains or lines available |
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| References |
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Original: |
J:42153
Haraguchi M et al.,
"Naturally occurring dermatitis associated with Staphylococcus aureus in DS-Nh mice."
Exp Anim 1997 Jul;46(3):225-9
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All: |
8 reference(s)
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Analysis Tools
