CFC1B
Cryptic family protein 1B
Also known as: CFC1B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P0CG36
- Gene
- CFC1B
- Ensembl
- ENSG00000152093
- Chromosome
- 2
- Canonical length
- 223 aa
- Protein class
- Predicted secreted proteins
- Secretome location
- Secreted - unknown location
OverviewNCBI Gene
Predicted to enable activin receptor binding activity and nodal binding activity. Predicted to be involved in circulatory system development; nodal signaling pathway; and regionalization. Predicted to act upstream of or within several processes, including heart development; left lung morphogenesis; and spleen development. Predicted to be active in cell surface and extracellular region. Implicated in tetralogy of Fallot and visceral heterotaxy. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
223 residues, UniProt reviewed canonical sequence.
>P0CG36|CFC1B
1 MTWRHHVRLL FTVSLALQII NLGNSYQREK HNGGREEVTK VATQKHRQSP LNWTSSHFGE
61 VTGSAEGWGP EEPLPYSWAF GEGASARPRC CRNGGTCVLG SFCVCPAHFT GRYCEHDQRR
121 SECGALEHGA WTLRACHLCR CIFGALHCLP LQTPDRCDPK DFLASHAHGP SAGGAPSLLL
181 LLPCALLHRL LRPDAPAHPR SLVPSVLQRE RRPCGRPGLG HRLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CFC1B can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.58
- Highest tissue expression
- 1.2 nTPM
Expression across tissuesHPA
Tissue
- pituitary gland: 1.2 nTPM
- hypothalamus: 0.6 nTPM
- pancreas: 0.6 nTPM
- prostate: 0.6 nTPM
- cerebellum: 0.3 nTPM
- basal ganglia: 0.2 nTPM
Single-cell type
- retinal bipolar cells: 1.3 nCPM
- fallopian tube ciliated cells: 0.4 nCPM
- pancreatic islet cells: 0.3 nCPM
- decidual stromal cells: 0.2 nCPM
- corticotrophs: 0.1 nCPM
- rod photoreceptor cells: 0.1 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- pons: 0.8 nTPM
- cerebral cortex: 0.6 nTPM
- medulla oblongata: 0.5 nTPM
- cerebellum: 0.1 nTPM
- hippocampal formation: 0.1 nTPM
- midbrain: 0.1 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- DepMap mean gene effect
- 0
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- anterior/posterior pattern specification
- blood vessel development
- determination of left/right symmetry
- gastrulation
- heart development
- nodal signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CFC1B as an antibody target. Whether an autoantibody or antibody against CFC1B could matter depends on whether native CFC1B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CFC1B is annotated as secreted, so native CFC1B circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label CFC1B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...