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EN
The tigrou-like mutation corresponds to a C-to-T transition at nucleotide position 3073, in exon 15 of 23 total exons, that results in replacement of alanine by valine at amino acid 999 of the protein. This is in the highly conserved sixth transmembrane domain that participates in formation of the cation channel. (J:133115, J:188598)
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
