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Gene | CSF3R |
Variant | E700* |
Impact List | nonsense |
Protein Effect | unknown |
Gene Variant Descriptions | CSF3R E700* results in a premature truncation of the Csf3r protein at amino acid 700 of 836 (UniProt.org). L700* results in increased Csf3r cell surface expression and impaired receptor internalization, however, leads to reduced Stat5 activation and G-CSF sensitivity compared to wild-type, and is not transforming in cell culture (PMID: 28439110), and therefore, its effect on Csf3r protein function is unknown. |
Associated Drug Resistance | |
Category Variants Paths |
CSF3R mutant CSF3R E700* |
Transcript | NM_000760.4 |
gDNA | chr1:g.36466770C>A |
cDNA | c.2098G>T |
Protein | p.E700* |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_172313 | chr1:g.36466770C>A | c.2098G>T | p.E700* | RefSeq | GRCh38/hg38 |
NM_000760.4 | chr1:g.36466770C>A | c.2098G>T | p.E700* | RefSeq | GRCh38/hg38 |
NM_172313.3 | chr1:g.36466770C>A | c.2098G>T | p.E700* | RefSeq | GRCh38/hg38 |
NM_000760.3 | chr1:g.36466770C>A | c.2098G>T | p.E700* | RefSeq | GRCh38/hg38 |
XM_005270493.1 | chr1:g.36466767C>A | c.2098G>T | p.E700* | RefSeq | GRCh38/hg38 |
XM_005270493 | chr1:g.36466767C>A | c.2098G>T | p.E700* | RefSeq | GRCh38/hg38 |
XM_005270493.1 | chr1:g.36466767C>A | c.2098G>T | p.E700* | RefSeq | GRCh38/hg38 |
NM_172313.2 | chr1:g.36466770C>A | c.2098G>T | p.E700* | RefSeq | GRCh38/hg38 |
NM_000760 | chr1:g.36466770C>A | c.2098G>T | p.E700* | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
CSF3R E700* | unknown |