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Gene | FGFR3 |
Variant | K508M |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | FGFR3 K508M lies within the protein kinase domain of the Fgfr3 protein (UniProt.org). K508M confers a loss of function to the Fgfr3 protein as demonstrated by induction of growth arrest in cell culture and inactivation of Stat1 in vitro (PMID: 19088846) and loss of kinase activity in the context of Fgfr3-Tacc3 (PMID: 22837387). |
Associated Drug Resistance | |
Category Variants Paths |
FGFR3 mutant FGFR3 inact mut FGFR3 K508M |
Transcript | NM_000142.5 |
gDNA | chr4:g.1805465A>T |
cDNA | c.1523A>T |
Protein | p.K508M |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_047449824.1 | chr4:g.1805465A>T | c.1523A>T | p.K508M | RefSeq | GRCh38/hg38 |
XM_006713873.1 | chr4:g.1805465A>T | c.1523A>T | p.K508M | RefSeq | GRCh38/hg38 |
NM_000142.4 | chr4:g.1805465A>T | c.1523A>T | p.K508M | RefSeq | GRCh38/hg38 |
XM_006713873 | chr4:g.1805465A>T | c.1523A>T | p.K508M | RefSeq | GRCh38/hg38 |
XM_006713873.2 | chr4:g.1805465A>T | c.1523A>T | p.K508M | RefSeq | GRCh38/hg38 |
NM_000142 | chr4:g.1805465A>T | c.1523A>T | p.K508M | RefSeq | GRCh38/hg38 |
XM_047449823.1 | chr4:g.1805465A>T | c.1523A>T | p.K508M | RefSeq | GRCh38/hg38 |
NM_000142.5 | chr4:g.1805465A>T | c.1523A>T | p.K508M | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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