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EN
The mutation, in exon 13 of the gene, comprises a T to C transition at nucleotide position 1491 of the cDNA sequence (ENSMUST00000027645). It is predicted to result in replacement of cysteine by arginine at nucleic acid position 465 of the protein (C465R). (J:104190)
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
