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Using an sgRNA (targeting GAATATGTAGGCAAGAGTTTGAAC) and ssODN template (TTCTTAGTTTTTGAGGCCAGCAGAAAGGAAGCCAGAATATGTAGGCAAGAGTTGGAACAGGTGAAAAGACGGAGGTACGATGCTTTCAGTCAATGTTTTGAACACATCTCAGTCTCAATTGATCAA) with CRISPR/Cas9 technology, phenylalanine codon 1054 (TTT) was changed to leucine (TTG) (c.3162T>G, p.F1054L). This is the equivalent of the human p.F1055L mutation caused by SNP rs61735519. (J:226562)
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
