Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 55997
MIM: 605194
HGNC: 18292
Ensembl: ENSG00000136698
Variants:
dbSNP: 55997
ClinVar: 55997
TCGA: ENSG00000136698
COSMIC: CFC1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000136698 | ENST00000259216 | P0CG37 |
| ENSG00000136698 | ENST00000615342 | A0A087WWV2 |
| ENSG00000136698 | ENST00000621673 | A0A087WX98 |
Expression (GTEx)
Pathways
| Pathway | Source | External ID |
|---|---|---|
| Developmental Biology | REACTOME | R-HSA-1266738 |
| Signaling by NODAL | REACTOME | R-HSA-1181150 |
| Regulation of signaling by NODAL | REACTOME | R-HSA-1433617 |
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 28620148 | 2017 | CFC1 is a cancer stemness-regulating factor in neuroblastoma. | 5 |
| 28620148 | 2017 | CFC1 is a cancer stemness-regulating factor in neuroblastoma. | 5 |
| 26476731 | 2016 | Cripto-1 modulates macrophage cytokine secretion and phagocytic activity via NF-κB signaling. | 9 |
| 27793090 | 2016 | Left-right axis asymmetry determining human Cryptic gene is transcriptionally repressed by Snail. | 1 |
| 26476731 | 2016 | Cripto-1 modulates macrophage cytokine secretion and phagocytic activity via NF-κB signaling. | 9 |
| 27793090 | 2016 | Left-right axis asymmetry determining human Cryptic gene is transcriptionally repressed by Snail. | 1 |
| 25423076 | 2015 | Duplication and deletion of CFC1 associated with heterotaxy syndrome. | 1 |
| 25423076 | 2015 | Duplication and deletion of CFC1 associated with heterotaxy syndrome. | 1 |
| 19853937 | 2011 | CFC1 mutations in Chinese children with congenital heart disease. | 7 |
| 19853937 | 2011 | CFC1 mutations in Chinese children with congenital heart disease. | 7 |
| 19853937 | 2011 | CFC1 mutations in Chinese children with congenital heart disease. | 7 |
| 19853937 | 2011 | CFC1 mutations in Chinese children with congenital heart disease. | 7 |
| 20634891 | 2010 | Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia. | 28 |
| 20634891 | 2010 | Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia. | 28 |
| 18162845 | 2008 | CFC1 gene involvement in biliary atresia with polysplenia syndrome. | 29 |
Citation
Dessen P
CFC1 (cripto, FRL-1, cryptic family 1)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/61768/cfc1-(cripto-frl-1-cryptic-family-1)
