CFC1 (cripto, FRL-1, cryptic family 1)

2014-11-01  

Identity

HGNC
LOCATION
2q21.1
LOCUSID
ALIAS
CFC1B,CRYPTIC,DTGA2,HTX2

Other Information

Locus ID:

NCBI: 55997
MIM: 605194
HGNC: 18292
Ensembl: ENSG00000136698

Variants:

dbSNP: 55997
ClinVar: 55997
TCGA: ENSG00000136698
COSMIC: CFC1

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000136698ENST00000259216P0CG37
ENSG00000136698ENST00000615342A0A087WWV2
ENSG00000136698ENST00000621673A0A087WX98

Expression (GTEx)

0
1
2
3
4
5
6
7
8
9
10

Pathways

PathwaySourceExternal ID
Developmental BiologyREACTOMER-HSA-1266738
Signaling by NODALREACTOMER-HSA-1181150
Regulation of signaling by NODALREACTOMER-HSA-1433617

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
286201482017CFC1 is a cancer stemness-regulating factor in neuroblastoma.5
286201482017CFC1 is a cancer stemness-regulating factor in neuroblastoma.5
264767312016Cripto-1 modulates macrophage cytokine secretion and phagocytic activity via NF-κB signaling.9
277930902016Left-right axis asymmetry determining human Cryptic gene is transcriptionally repressed by Snail.1
264767312016Cripto-1 modulates macrophage cytokine secretion and phagocytic activity via NF-κB signaling.9
277930902016Left-right axis asymmetry determining human Cryptic gene is transcriptionally repressed by Snail.1
254230762015Duplication and deletion of CFC1 associated with heterotaxy syndrome.1
254230762015Duplication and deletion of CFC1 associated with heterotaxy syndrome.1
198539372011CFC1 mutations in Chinese children with congenital heart disease.7
198539372011CFC1 mutations in Chinese children with congenital heart disease.7
198539372011CFC1 mutations in Chinese children with congenital heart disease.7
198539372011CFC1 mutations in Chinese children with congenital heart disease.7
206348912010Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.28
206348912010Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.28
181628452008CFC1 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