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Muc13m1Wtsi
Spontaneous Allele Detail
Summary
Symbol: Muc13m1Wtsi
Name: mucin 13, epithelial transmembrane; mutation 1, Wellcome Trust Sanger Institute
MGI ID: MGI:7565306
Synonyms: Muc3sp
Gene: Muc13  Location: Chr16:33614407-33640299 bp, + strand  Genetic Position: Chr16, 24.21 cM
Alliance: Muc13m1Wtsi page
Mutation
origin
Strain of Origin:  C57BL/6N-Atm1Brd
Mutation
description
Allele Type:    Spontaneous (No functional change)
Mutation:    Single point mutation
 
Mutation detailsA spontaneous mutation produces the amino acid substitution of arginine with tryptophan at position 334 (Arg334Trp). (J:327181)
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 Muc13 Mutation:  21 strains or lines available
References
Original:  J:327181 Lewis MA, et al., Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme. BMC Biol. 2022 Mar 17;20(1):67
All:  1 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
11/19/2024
MGI 6.24
The Jackson Laboratory