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Inpp5del20
Chemically induced Allele Detail
Summary
Symbol: Inpp5del20
Name: inositol polyphosphate-5-phosphatase D; early lethal
MGI ID: MGI:5050823
Synonyms: Ship1el20
Gene: Inpp5d  Location: Chr1:87548034-87648229 bp, + strand  Genetic Position: Chr1, 44.44 cM, cytoband C5
Alliance: Inpp5del20 page
Mutation
origin
Strain of Origin:  129
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsA T to C transition was found at nucleotide position 2099 (Genbank NM_010566) in ENU mutant mice. This should cause an isoleucine to threonine change at amino acid residue 641. An in-vitro 5'-phosphatase assay demonstrated reduced enzyme activity as compared to un-mutated controls. Protein levels were reduced in Western blots as were mRNA levels by qRT-PCR. (J:173266)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 anatomical structure(s)
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 Inpp5d Mutation:  94 strains or lines available
References
Original:  J:173266 Nguyen NY, et al., An ENU-induced mouse mutant of SHIP1 reveals a critical role of the stem cell isoform for suppression of macrophage activation. Blood. 2011 May 19;117(20):5362-71
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