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PrkcbM4Btlr
Chemically induced Allele Detail
Summary
Symbol: PrkcbM4Btlr
Name: protein kinase C, beta; mutation 4, Bruce Beutler
MGI ID: MGI:6305123
Synonyms: Mesopotamia
Gene: Prkcb  Location: Chr7:121888327-122233625 bp, + strand  Genetic Position: Chr7, 65.75 cM
Alliance: PrkcbM4Btlr page
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Beutler Mutagenetix
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsENU-induced T to C transition at base pair 122,289,514 (v38) on chromosome 7, or base pair 390 in the GenBank genomic region NC_000073. The mutation corresponds to residue 390 in the mRNA sequence NM_008855 within exon 1 of 17 total exons. The mutation results in an isoleucine to threonine substitution at position 57 (I57T) in the PKC protein. (J:274860)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Prkcb Mutation:  39 strains or lines available
Notes
https://mutagenetix.utsouthwestern.edu/phenotypic/phenotypic_rec.cfm?pk=4260
References
Original:  J:274860 Choi JH, et al., Mutagenetix entry for Mesopotamia. MGI Direct Data Submission. 2019;
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
12/10/2024
MGI 6.24
The Jackson Laboratory