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Krt71Ca
Spontaneous Allele Detail
Nomenclature
Symbol: Krt71Ca
Name: keratin 71; caracul
MGI ID: MGI:1855990
Synonyms: Ca
Gene: Krt71  Location: Chr15:101733949-101743097 bp, - strand  Genetic Position: Chr15, 57.0 cM
Mutation
origin
Strain of Origin:  Swiss stock
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsSequence analysis identified the transversion of an C-to-A at coding nucleotide 1292, resulting in an alanine to aspartic acid missense mutation at codon 431 (p.A431D).
Inheritance:    Dominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Krt71 Mutation:  11 strains or lines available
References
Original:  J:13054 Dunn LC, Caracul, a dominant mutation. J Hered. 1937;28:334
All:  6 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
04/06/2021
MGI 6.16
The Jackson Laboratory