RAP2A
Ras-related protein Rap-2a
Also known as: K-REV, RAP2, RAP2A_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P10114
- Gene
- RAP2A
- Ensembl
- ENSG00000125249
- Chromosome
- 13
- Canonical length
- 183 aa
- Protein class
- Enzymes, Predicted intracellular proteins
OverviewNCBI Gene
Enables GTPase activity; guanyl ribonucleotide binding activity; and magnesium ion binding activity. Involved in several processes, including microvillus assembly; positive regulation of protein autophosphorylation; and regulation of dendrite morphogenesis. Acts upstream of or within establishment of protein localization. Located in plasma membrane and recycling endosome membrane. Is active in Schaffer collateral - CA1 synapse. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
183 residues, UniProt reviewed canonical sequence.
>P10114|RAP2A
1 MREYKVVVLG SGGVGKSALT VQFVTGTFIE KYDPTIEDFY RKEIEVDSSP SVLEILDTAG
61 TEQFASMRDL YIKNGQGFIL VYSLVNQQSF QDIKPMRDQI IRVKRYEKVP VILVGNKVDL
121 ESEREVSSSE GRALAEEWGC PFMETSAKSK TMVDELFAEI VRQMNYAAQP DKDDPCCSAC
181 NIQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RAP2A 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 41 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 41 nTPM
- spinal cord: 35 nTPM
- amygdala: 27 nTPM
- hippocampal formation: 25 nTPM
- midbrain: 24 nTPM
- placenta: 24 nTPM
Single-cell type
- microglia: 124 nCPM
- esophageal apical cells: 123 nCPM
- oligodendrocyte progenitor cells: 81 nCPM
- lactotrophs: 67 nCPM
- gonadotrophs: 67 nCPM
- cdc: 67 nCPM
Immune cell
- non-classical monocyte: 2 nTPM
- gdT-cell: 1.9 nTPM
- plasmacytoid DC: 1.6 nTPM
- naive CD8 T-cell: 1.5 nTPM
- intermediate monocyte: 1.4 nTPM
- memory CD8 T-cell: 1.4 nTPM
Brain region
- cerebral cortex: 62 nTPM
- basal ganglia: 59 nTPM
- hypothalamus: 58 nTPM
- white matter: 56 nTPM
- spinal cord: 50 nTPM
- midbrain: 46 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)
- 0.48
- gnomAD pLI
- 0.85
- gnomAD missense Z
- 2.56
- DepMap mean gene effect
- -0.1
- DepMap dependency class
- selective
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
- actin cytoskeleton organization
- establishment of protein localization
- intracellular protein localization
- negative regulation of cell migration
- positive regulation of cell migration
- positive regulation of microvillus assembly
- Rap protein signal transduction
- regulation of dendrite morphogenesis
- regulation of JNK cascade
- regulation of postsynaptic membrane neurotransmitter receptor levels
- regulation of synapse assembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RAP2A 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 RAP2A as an antibody target. Whether an autoantibody or antibody against RAP2A could matter depends on whether native RAP2A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RAP2A is annotated at the cell surface, where native RAP2A is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label RAP2A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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