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Using CRISPR/Cas9 technology and an sgRNA and an ssODN template oligonucleotide, an allele was created with a GC>AG mutation leading to a p.G167E substitution in the encoded peptide (equivalent to p.G169E in the human ortholog). (J:279291)
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
