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EN
The mutation, in exon 2 of the gene, has been identified as a C to T transition at nucleotide position 1079 of the cDNA sequence (ENSMUST00000078494) that converts a triplet encoding arginine at amino acid position 328 to a termination codon (R328Ter). (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
