Difference between revisions of "Part:BBa K2961000"
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− | This part encodes for a | + | This part encodes for a sequence that is a segment that is specific to the CFTR gene, but specifically SNP variant rs75389940_G, which is a common allele in the Middle East responsible for the prevalence of cystic fibrosis. |
− | This part | + | This part has been designed to strategically be a copy of a segment of the CFTR gene that is close to the PAM site for Cpf1, so that it may be used for targeting through gRNA design. |
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Latest revision as of 01:41, 17 October 2019
CFTR Mutant Gene Segment (rs75389940_G)
This part encodes for a sequence that is a segment that is specific to the CFTR gene, but specifically SNP variant rs75389940_G, which is a common allele in the Middle East responsible for the prevalence of cystic fibrosis.
This part has been designed to strategically be a copy of a segment of the CFTR gene that is close to the PAM site for Cpf1, so that it may be used for targeting through gRNA design.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]