Log In|Sign Up
EN
A failed complementation test of this spontaneous mutant with the Npr2cn-2J allele demonstrated that this mutation is an allele of Npr2, and a G-to-A transition was identified in chromosome 4 position 43650227 (GRCm38), which is in exon 19 and causes an alanine to threonine substitution at position 931 (p.A931T). (J:170669)
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
