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EN
A loxP flanked neomycin selection cassette and exon 17 containing an arginine to glutamine substitution at amino acid 617 (c.1850G>A, p.R617Q) replaced exon 17, which corresponds to c.1841G>A, p.R614Q in the mouse on GRCm39. The p.R617Q missense mutation was reported in a familial intellectual disability disorder. (J:334076)
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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References Literature
Title
PMID
Journal
Year
IF
