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Tpi1a-m6Neu
Chemically induced Allele Detail
Summary
Symbol: Tpi1a-m6Neu
Name: triosephosphate isomerase 1; mutation 6, Neuherberg
MGI ID: MGI:4821798
Gene: Tpi1  Location: Chr6:124787549-124791121 bp, - strand  Genetic Position: Chr6, 59.17 cM
Alliance: Tpi1a-m6Neu page
Mutation
origin
Strain of Origin:  (101/El x C3H/El)F1
Mutation
description
Allele Type:    Chemically induced (other)
Mutation:    Single point mutation
 
Mutation detailsTriethylenemelamine mutagenesis induced an A to G transition at position 149 of exon 2 (GenBank/EMBL accession number NM009415) that results in the amino acid substitution of glycine for aspartic acid at position 49 (D49G). Triosephosphate isomerase activity in the blood, lung, spleen, heart, liver, kidney, and brain is reduced in heterozygotes and homozygotes. (J:163223)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Tpi1 Mutation:  23 strains or lines available
References
Original:  J:163223 Pretsch W, Triosephosphate isomerase activity-deficient mice show haemolytic anaemia in homozygous condition. Genet Res. 2009 Feb;91(1):1-4
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