三甲胺联苯胺诱发的突变在NM009415基因的第149位,从A变为G(在exon 2),导致第49位的氨基酸从甘氨酸替换为天冬氨酸(D49G)。在血液、肺、脾、心、肝、肾和脑中的三磷酸异构酶活性在杂合子和纯合子中都降低。(来源:J:163223)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
(101/El x C3H/El)F1
Chemically induced
单点
隐性
1
1
1

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

References Literature

Title
PMID
Journal
Year
IF
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