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The mutation has been identified as a T to C transition at nucleotide position 673 of the transcript (NM_011616.2 from NCBI Build 37.1), in the last of the gene's 5 exons. It is predicted to result in replacement of serine by proline at amino acid position 221 of the protein, in the tumor necrosis factor (TNF)-like extracellular region. (J:162147)
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
