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Triethylenemelamine 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)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
