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The mutation is an A-to-T transversion at nucleotide position 813, in the last of 6 exons, resulting in replacement of isoleucine by phenylalanine at amino acid position 105 (I105F), at the N-terminal border of the death domain of the protein. (J:133274)
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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References Literature
Title
PMID
Journal
Year
IF
