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EN
ENU-induced T to C transition at base pair 30,599,743 (v38) on chromosome 14, or base pair 26,672 in the GenBank genomic region NC_000080 encoding Prkcd. The mutation corresponds to residue 1,501 in the mRNA sequence NM_001310682 within exon 14 of 17 total exons. The mutated nucleotide is indicated in red. The mutation results in a leucine to proline substitution at position 498 (L498P) in variant 1 of the PRKCD protein. (J:265146)
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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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
