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An A-to-T mutation at coding nucleotide 115 of the encoded mRNA (c.115A>T) that altered codon 39 from a lysine to a stop codon (p.K39*). If the peptide is translated, it will lack the domains required for guanine nucleotide and Rab effector binding. (J:70423)
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
