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EN
A spontaneous G-to-A point mutation at 92,250,964 of Chr15 (GRCm38) changes tryptophan codon 364 into a premature stop codon at position 364 (p.W364*). Western blot of brain or spinal cord extracts from homozygotes failed to identify this protein and efforts to amplify segments of this gene from cDNA failed. (J:178817, J:222308)
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
