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An A-to-G mutation at coding nucleotide 1165 resulted in an arginine to glycine substitution at amino acid position 389 (p.R389G). This mutation is within the second of four zinc finger domains and affects a residue predicted to interact directly with DNA. (J:95867)
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：
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References Literature
Title
PMID
Journal
Year
IF
