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

Symbol:	Krt71Ca-9J
Name:	keratin 71; caracul 9 Jackson
MGI ID:	MGI:1855993
Gene:	Krt71  Location: Chr15:101642384-101651532 bp, - strand  Genetic Position: Chr15, 57.0 cM
Alliance:	Krt71Ca-9J page

Strain of Origin:

BALB/cBy

Allele Type:    Spontaneous Mutation:    Intragenic deletion   Mutation details: Sequence analysis identified the spontaneous deletion of asparagine codon 139 or 140, through the deletion of CAA / ACA / AAC from the AACAACAA sequence at codong nucleotides 415-422. The deleted codon is located in the alpha-helical rod domain. This molecular lesion is the same that has been identified in Krt71Ca-Rin, Krt71Ca-J, and Krt71Ca-10J. Inheritance:    Dominant

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:30778 Sweet HO, et al., Remutations at The Jackson Laboratory (Update to Mouse Genome 1993; 91:862-5 - J16313). Mouse Genome. 1995;93(4):1030-4
All:	2 reference(s)