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Sequencing of all exons of the gene identified a T-to-C transition in exon 2 that results in substitution of phenylalanine (TTT) with serine (TCT) in this very highly evolutionarily conserved protein. Failure to complement another mutation at this locus, underwhite 5 Jackson, verified responsibility of these mutations for the observed phenotype. (J:112289)
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
