ENU mutagenesis induced a mis-sense (A to G) mutation at nucleotide 1862 (accession #BC060704) that results in the amino acid substitution of glycine for aspartic acid at position 549 (D549G). (J:170646)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C3H.Cg-Foxq1sa/H
Chemically induced
Single point
Semidominant
1
5
3

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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