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CRISPR/Cas9 technology generated a C to G change resulting in a phenylalanine to leucine substitution at amino acid 218 (p.F218L). This is equivalent to the human p.F234L pathogenic variant identified in a Pakistani family with Goldenhar syndrome (craniofacial microsomia). (J:336768)
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
