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EN
CRISPR/cas9 guide RNA sequences (CCTGGTGAACCTGGTCAAGC and CCAGGGGGACCTTGGTATC) are targeted to exon 7 to introduce a glycine to serine substitution in amino acid 209 (G209S; nucleotide change GGT to TCT). The mutation is located at the beginning of the triple helical collagenous domain. This mutation is analogous to one found in Vascular Ehlers-Danlos syndrome (vEDS) patients. (J:312454)
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
