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CRISPR/cas9 genome editing uses guide RNAs (CCCTCTGTGCAGTGGGACCA, GTGCAGTGGGACCAAGGCTC, and AGTCTCACCGGCCTGAGCCT) were selected to target exon 11. Donor DNAs were created encoding a Q306X mutation (CAA to TGA, glutamine to stop). The orthologous clinical mutation R306X is associated with hereditary spastic paraplegia. (J:94077)
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
