Log In|Sign Up
EN
CRISPR/Cas9 technology generated a TGG to CGC change resulting in a tryptophan to arginine substitution at amino acid 230 (W230R). This change corresponds to the W231R variant found in a pediatric patient with X-linked familial autoinflammatory syndrome. (J:328935)
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
