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Sppl2achompB
Chemically induced Allele Detail
Summary
Symbol: Sppl2achompB
Name: signal peptide peptidase like 2A; chompB
MGI ID: MGI:5484577
Gene: Sppl2a  Location: Chr2:126732311-126775155 bp, - strand  Genetic Position: Chr2, 61.76 cM, cytoband F3
Alliance: Sppl2achompB page
Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Chemically induced (ENU) (Hypomorph)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a T to A transversion that results in the amino acid substitution of lysine for methionine at position 252 (M252K) in the third transmembrane domain. This allele is hypomorphic. (J:194595)
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 Sppl2a Mutation:  47 strains or lines available
References
Original:  J:194595 Beisner DR, et al., The intramembrane protease Sppl2a is required for B cell and DC development and survival via cleavage of the invariant chain. J Exp Med. 2013 Jan 14;210(1):23-30
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
11/12/2024
MGI 6.24
The Jackson Laboratory