Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	Krt71Rgsc689
Name:	keratin 71; RIKEN Genomic Sciences Center (GSC), 689
MGI ID:	MGI:2681099
Synonyms:	Krt2-6g1Rgsc, M100689
Gene:	Krt71  Location: Chr15:101642384-101651532 bp, - strand  Genetic Position: Chr15, 57.0 cM
Alliance:	Krt71Rgsc689 page

Strain of Origin:	C57BL/6J
Project Collection:	RIKEN GSC ENU Project

Allele Type:    Chemically induced (ENU) Mutation:    Single point mutation   Mutation details: Sequence analysis of Krt2-6g in this mouse identified the transversion of an thymine to a guanine at nucleotide 1271, resulting in a leucine to tryptophan missense mutation at codon 424 (L424W). (J:86407) Inheritance:    Dominant

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

2 anatomical structure(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Krt71 Mutation:	43 strains or lines available

Original:	J:86407 Kikkawa Y, et al., A small deletion hotspot in the type II keratin gene mK6irs1/Krt2-6g on mouse chromosome 15, a candidate for causing the wavy hair of the caracul (Ca) mutation. Genetics. 2003 Oct;165(2):721-33
All:	2 reference(s)