Log In|Sign Up
EN
CRISPR/Cas9 technology generated a single nucleotide change of G to A, resulting in an alanine to threonine change at amino acid 778 (p.A778T). This corresponds to the human A786T mutation associated with an increased risk of developing an eating disorder. (J:280111)
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
