CFC1

GENERAL INFORMATION

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Gene name

CFC1

Gene description

Cripto, FRL-1, cryptic family 1

Protein class

Disease related genes
Predicted secreted proteins

Predicted localization

Secreted

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Group enriched (pancreas, prostate, stomach)
GTEx:Tissue enhanced (pancreas, stomach)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic and membranous positivity in several tissues.

ANTIBODY RELIABILITY

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Data reliability
description

Caution, targets protein from more than one gene. Secreted protein, tissue location of RNA and protein might differ and correlation is complex.

Data reliability

Uncertain based on 1 antibody.
HPA041773
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Pancreas

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Group enriched (pancreas, prostate, stomach)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (pancreas, stomach)

Organ

Expression



GENE INFORMATION

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Gene name

CFC1 (HGNC Symbol)

Synonyms

CRYPTIC, HTX2

Description

Cripto, FRL-1, cryptic family 1 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the epidermal growth factor (EGF)- Cripto, Frl-1, and Cryptic (CFC) family, which are involved in signalling during embryonic development. Proteins in this family share a variant EGF-like motif, a conserved cysteine-rich domain, and a C-terminal hydrophobic region. The protein encoded by this gene is necessary for patterning the left-right embryonic axis. Mutations in this gene are associated with defects in organ development, including autosomal visceral heterotaxy and congenital heart disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]

Chromosome

2

Cytoband

q21.1

Chromosome location (bp)

130592168 - 130599575

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000136698 (version 78.38)

Entrez gene

55997

UniProt

P0CG37 (UniProt - Evidence at protein level)

neXtProt

NX_P0CG37

Antibodypedia

CFC1 antibodies


PROTEIN BROWSER

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ENST00000259216
 
ENST00000615342
 
ENST00000621673
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

CFC1-001 ENSP00000259216
ENST00000259216
P0CG37
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Show » Show » 223 24.6 Yes 0
CFC1-201 ENSP00000480526
ENST00000615342
Show » 191 20.3 Yes 0
CFC1-202 ENSP00000480843
ENST00000621673
Show » 148 16.4 Yes 0