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Immp2lm1Btlr
Chemically induced Allele Detail
Summary
Symbol: Immp2lm1Btlr
Name: IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae); mutation 1, Bruce Beutler
MGI ID: MGI:5806308
Synonyms: imp
Gene: Immp2l  Location: Chr12:41074089-42002371 bp, + strand  Genetic Position: Chr12, 18.69 cM, cytoband B3
Alliance: Immp2lm1Btlr 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 A transversion at base pair 41,110,847 (v38) on chromosome 12, or base pair 86,758 in the GenBank genomic region NC_000078. The mutation corresponds to residue 274 in the NM_053122 mRNA sequence in exon 4 of 7 total exons. The mutation results in substitution of leucine (L) 48 to a premature stop codon (L48*) in the coded protein. (J:236672)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
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 Immp2l Mutation:  27 strains or lines available
References
Original:  J:236672 Chen Z, et al., Mutagenetix entry for imp. MGI Direct Data Submission. 2016;
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
04/23/2024
MGI 6.23
The Jackson Laboratory