Log In|Sign Up
EN
ENU-induced C to T transition at base pair 122,627,693 (v38) on chromosome 7, or base pair 338,569 in the GenBank genomic region NC_000073. The mutation corresponds to residue 2,121 in the mRNA sequence NM_008855 within exon 17 of 17 total exons. The mutation results in a threonine to isoleucine substitution at position 634 (T634I) in the PKC protein. (J:274861)
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
