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Krt25Rgsc573
Chemically induced Allele Detail
Summary
Symbol: Krt25Rgsc573
Name: keratin 25; RIKEN Genomic Sciences Center (GSC), 573
MGI ID: MGI:3707007
Synonyms: M100573
Gene: Krt25  Location: Chr11:99206342-99213777 bp, - strand  Genetic Position: Chr11, 62.92 cM
Alliance: Krt25Rgsc573 page
Mutation
origin
Strain of Origin:  (DBA/2J x C57BL/6J)F1
Project Collection: RIKEN GSC ENU Project
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Nucleotide substitutions
 
Mutation detailsThis allele contains a single nonsynonymous base substitution , 1135 T to A, that results in an amino acid substitution of asparagine for tyrosine at position 379 (Y379N). (J:130100)
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 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 Krt25 Mutation:  28 strains or lines available
References
Original:  J:130597 Masuya H, et al., Implementation of the modified-SHIRPA protocol for screening of dominant phenotypes in a large-scale ENU mutagenesis program. Mamm Genome. 2005 Nov;16(11):829-37
All:  3 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