RBPMS2
RNA-binding protein with multiple splicing 2
Also known as: RBPS2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6ZRY4
- Gene
- RBPMS2
- Ensembl
- ENSG00000166831
- Chromosome
- 15
- Canonical length
- 209 aa
- Protein class
- Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
The protein encoded by this gene is a member of the RNA recognition motif (RRM)-containing protein family and is involved in the development and dedifferentiation of digestive smooth muscle cells. The encoded protein functions as a homodimer and indirectly inhibits the bone morphogenetic protein pathway. [provided by RefSeq, Aug 2016]
Canonical amino-acid sequenceUniProt
209 residues, UniProt reviewed canonical sequence.
>Q6ZRY4|RBPMS2
1 MSNLKPDGEH GGSTGTGSGA GSGGALEEEV RTLFVSGLPV DIKPRELYLL FRPFKGYEGS
61 LIKLTARQPV GFVIFDSRAG AEAAKNALNG IRFDPENPQT LRLEFAKANT KMAKSKLMAT
121 PNPSNVHPAL GAHFIARDPY DLMGAALIPA SPEAWAPYPL YTTELTPAIS HAAFTYPTAT
181 AAAAALHAQV RWYPSSDTTQ QGWKYRQFCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RBPMS2 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.58
- Highest tissue expression
- 284 nTPM
Expression across tissuesHPA
Tissue
- heart muscle: 284 nTPM
- blood vessel: 138 nTPM
- colon: 138 nTPM
- urinary bladder: 92 nTPM
- endometrium: 49 nTPM
- stomach: 48 nTPM
Single-cell type
- megakaryocytes: 420 nCPM
- vascular smooth muscle cells: 136 nCPM
- smooth muscle cells: 126 nCPM
- platelets: 126 nCPM
- megakaryocyte progenitors: 95 nCPM
- parietal cells: 69 nCPM
Immune cell
- naive B-cell: 0.7 nTPM
- memory B-cell: 0.4 nTPM
- total PBMC: 0.4 nTPM
- NK-cell: 0.2 nTPM
- memory CD8 T-cell: 0.1 nTPM
- basophil: 0 nTPM
Brain region
- choroid plexus: 29 nTPM
- thalamus: 24 nTPM
- cerebral cortex: 11 nTPM
- amygdala: 8.7 nTPM
- midbrain: 8.3 nTPM
- hypothalamus: 6.7 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)
- 0.42
- gnomAD pLI
- 0.88
- gnomAD missense Z
- 0.94
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- embryonic digestive tract morphogenesis
- negative regulation of BMP signaling pathway
- negative regulation of smooth muscle cell differentiation
- positive regulation of smooth muscle cell proliferation
- regulation of alternative mRNA splicing, via spliceosome
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RBPMS2 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 RBPMS2 as an antibody target. Whether an autoantibody or antibody against RBPMS2 could matter depends on whether native RBPMS2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RBPMS2 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 RBPMS2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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