RAP2C
Ras-related protein Rap-2c
Also known as: DKFZp313B211, RAP2C_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y3L5
- Gene
- RAP2C
- Ensembl
- ENSG00000123728
- Chromosome
- X
- Canonical length
- 183 aa
- Protein class
- Enzymes, Predicted intracellular proteins
OverviewNCBI Gene
The protein encoded by this gene is a member of the Ras-related protein subfamily of the Ras GTPase superfamily. Members of this family are small GTPases that act as molecular switches to regulate cellular proliferation, differentiation, and apoptosis. This protein has been reported to activate in vitro transcriptional activity of the serum response element. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2012]
Canonical amino-acid sequenceUniProt
183 residues, UniProt reviewed canonical sequence.
>Q9Y3L5|RAP2C
1 MREYKVVVLG SGGVGKSALT VQFVTGTFIE KYDPTIEDFY RKEIEVDSSP SVLEILDTAG
61 TEQFASMRDL YIKNGQGFIL VYSLVNQQSF QDIKPMRDQI VRVKRYEKVP LILVGNKVDL
121 EPEREVMSSE GRALAQEWGC PFMETSAKSK SMVDELFAEI VRQMNYSSLP EKQDQCCTTC
181 VVQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RAP2C 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 86 nTPM
Expression across tissuesHPA
Tissue
- endometrium: 86 nTPM
- smooth muscle: 52 nTPM
- bone marrow: 50 nTPM
- liver: 44 nTPM
- epididymis: 29 nTPM
- lymph node: 25 nTPM
Single-cell type
- neutrophils: 203 nCPM
- cardiomyocytes: 180 nCPM
- syncytiotrophoblasts: 86 nCPM
- neutrophil progenitors: 74 nCPM
- esophageal apical cells: 66 nCPM
- monocytes: 61 nCPM
Immune cell
- non-classical monocyte: 15 nTPM
- eosinophil: 11 nTPM
- intermediate monocyte: 8.9 nTPM
- neutrophil: 8.1 nTPM
- basophil: 6.8 nTPM
- NK-cell: 6.8 nTPM
Brain region
- medulla oblongata: 17 nTPM
- hypothalamus: 16 nTPM
- spinal cord: 16 nTPM
- thalamus: 15 nTPM
- white matter: 15 nTPM
- midbrain: 14 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.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.19
- gnomAD pLI
- 0.3
- gnomAD missense Z
- 1.73
- DepMap mean gene effect
- 0.12
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- establishment of endothelial intestinal barrier
- negative regulation of cell migration
- Rap protein signal transduction
- regulation of protein tyrosine kinase activity
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RAP2C in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads RAP2C as an antibody target. Whether an autoantibody or antibody against RAP2C could matter depends on whether native RAP2C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RAP2C is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label RAP2C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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