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Prf1m1Btlr
Chemically induced Allele Detail
Summary
Symbol: Prf1m1Btlr
Name: perforin 1 (pore forming protein); mutation 1, Bruce Beutler
MGI ID: MGI:5607639
Synonyms: prime
Gene: Prf1  Location: Chr10:61133612-61140459 bp, + strand  Genetic Position: Chr10, 32.18 cM
Alliance: Prf1m1Btlr 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 detailsThe molecular lesion is a C to A transversion at base pair 61,303,722 (v38) on chromosome 10, or base pair 6,045 in the GenBank genomic region NC_000076. This corresponds to nucleotide 1,513 in the mRNA sequence NM_011073, within exon 3 of 3 total exons. The mutation results in substitution of a premature stop codon for a tyrosine at residue 486 (Y486Ter). (J:216044)
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Prf1 Mutation:  48 strains or lines available
References
Original:  J:216044 Zhang D, et al., Mutagenetix entry for prime. Updated on December 15, 2014. MGI Direct Data Submission. 2014;
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
04/16/2024
MGI 6.23
The Jackson Laboratory