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A chr7:102421471A>T (GRCm38.p4) point mutation was generated using zinc finger nuclease and a repair oligodinucleotide. This mutation changes arginine codon 304 to a tryptophan codon (p.R304W) and is found in Stormorken syndrome patients. Immunohistochemistry experiments showed protein expression from this allele. (J:293834)
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
