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An ENU mutagenesis induced a C-to-T transition at base pair chr9:75161492 (GRCm38). The mutation corresponds to residue 2402 in the mRNA sequence NM_010864 within exon 2 of 17 total exons. The mutation results in an arginine to cysteine substitution at amino acid 659 (p.R659C). (J:201726)
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
