ENU-induced T to C transition at base pair 20,508,543 (v38) on chromosome 14, or base pair 38,031 in the GenBank genomic region NC_000080 encoding Ppp3cb. The mutation corresponds to residue 1,450 in the cDNA sequence ENSMUST00000022355.10 within exon 12 of 12 total exons. The mutation results in a cysteine to arginine substitution at position 484 (C484R) in an alternative 497-amino acid isoform of CnAbeta. The effect of the mutation at the cDNA and protein levels has not been examined, but the mutation is within intron 12 (81-base pairs from exon 12) in the canonical isoform of Ppp3cb; the mutation is not predicted to affect splicing of the transcript. (J:272839)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6J
Chemically induced
Single point
Recessive
1
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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

References Literature

Title
PMID
Journal
Year
IF
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