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Prkcem1Btlr
Chemically induced Allele Detail
Summary
Symbol: Prkcem1Btlr
Name: protein kinase C, epsilon; mutation 1, Bruce Beutler
MGI ID: MGI:6269444
Synonyms: pinnacles
Gene: Prkce  Location: Chr17:86475213-86965347 bp, + strand  Genetic Position: Chr17, 56.74 cM
Alliance: Prkcem1Btlr 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 C to T transition at base pair 86,476,851 (v38) on chromosome 17, or base pair 309,298 in the GenBank genomic region NC_000083 encoding Prkce. The mutation corresponds to residue 1,461 in the mRNA sequence NM_011104 within exon 5 of 15 total exons. The mutation results in a threonine (T) to isoleucine (I) substitution at position 218 (T218I) in the PKC protein. (J:267703)
Inheritance:    Recessive
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 Prkce Mutation:  40 strains or lines available
References
Original:  J:267703 Zhong X, et al., Mutagenetix entry for pinnacles. MGI Direct Data Submission. 2018;
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
10/29/2024
MGI 6.24
The Jackson Laboratory