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Trpv3Nh
Spontaneous Allele Detail
Nomenclature
Symbol: Trpv3Nh
Name: transient receptor potential cation channel, subfamily V, member 3; non-hair
MGI ID: MGI:2384170
Gene: Trpv3  Location: Chr11:73267388-73300363 bp, + strand  Genetic Position: Chr11, 45.25 cM
Mutation
origin
Strain of Origin:  DS
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsA 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)
Inheritance:    Dominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 1 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 3 strains available      Cell Lines: 0 lines available
Carrying any Trpv3 Mutation:  29 strains or lines available
References
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
All:  8 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/12/2018
MGI 6.12
The Jackson Laboratory