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This mutation, originally identified in an ENU mutagenesis screen by its visible phenotype, is due to an A-to-T transversion in exon 6 resulting in substitution of asparagine for isoleucine at amino acid position 273 of the protein (I273N), which alters the ligand binding and heterodimerization domain. (J:103186)
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
