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Gene | TSC2 |
Variant | R1743W |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | TSC2 R1743W lies within the Rap-GAP domain of the Tsc2 protein (UniProt.org). R1743W results in the loss of repression of mTORC1 as demonstrated by increased phosphorylation of S6K1 and 4E-BP1, reduced intrinsic GTPase activity, and PEX5 association and peroxisomal localization compared to wild-type Tsc2 protein in in-vitro assays (PMID: 23955302). |
Associated Drug Resistance | |
Category Variants Paths |
TSC2 mutant TSC2 inact mut TSC2 R1743W |
Transcript | NM_000548.5 |
gDNA | chr16:g.2088293C>T |
cDNA | c.5227C>T |
Protein | p.R1743W |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000548 | chr16:g.2088293C>T | c.5227C>T | p.R1743W | RefSeq | GRCh38/hg38 |
NM_000548.4 | chr16:g.2088293C>T | c.5227C>T | p.R1743W | RefSeq | GRCh38/hg38 |
NM_000548.5 | chr16:g.2088293C>T | c.5227C>T | p.R1743W | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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