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Krt27stpm
Spontaneous Allele Detail
Summary
Symbol: Krt27stpm
Name: keratin 27; short term perm
MGI ID: MGI:3522000
Gene: Krt27  Location: Chr11:99236391-99241930 bp, - strand  Genetic Position: Chr11, 62.92 cM
Alliance: Krt27stpm page
Three week old Krt27stpm/Krt27stpm

Show the 2 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  RHJ/LeJ
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsThis spontaneous mutation arose at The Jackson Laboratory. A T-to-C point mutation at coding nucleotide 965 of the cDNA (NM_010666) results in a leucine to proline substitution at position 322 of the encoded protein (p.L322P). (J:222308)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structure(s)
Find Mice (IMSR)
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 Krt27 Mutation:  18 strains or lines available
References
Original:  J:100186 Samples RM, et al., Short term perm (stpm): a new recessive curly coat mutation. MGI Direct Data Submission. 2005;
All:  2 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
04/23/2024
MGI 6.23
The Jackson Laboratory