ESRP2
Epithelial splicing regulatory protein 2
Also known as: ESRP2_HUMAN, FLJ21918, RBM35B
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H6T0
- Gene
- ESRP2
- Ensembl
- ENSG00000103067
- Chromosome
- 16
- Canonical length
- 727 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
ESPR2 is an epithelial cell-type-specific splicing regulator (Warzecha et al., 2009 [PubMed 19285943]).[supplied by OMIM, Aug 2009]
Canonical amino-acid sequenceUniProt
727 residues, UniProt reviewed canonical sequence.
>Q9H6T0|ESRP2
1 MTPPPPPPPP PGPDPAADPA ADPCPWPGSL VVLFGATAGA LGRDLGSDET DLILLVWQVV
61 EPRSRQVGTL HKSLVRAEAA ALSTQCREAS GLSADSLARA EPLDKVLQQF SQLVNGDVAL
121 LGGGPYMLCT DGQQLLRQVL HPEASRKNLV LPDMFFSFYD LRREFHMQHP STCPARDLTV
181 ATMAQGLGLE TDATEDDFGV WEVKTMVAVI LHLLKEPSSQ LFSKPEVIKQ KYETGPCSDS
241 TVPCPYSSKA DVVDSETVVR ARGLPWQSSD QDVARFFKGL NVARGGVALC LNAQGRRNGE
301 ALIRFVDSEQ RDLALQRHKH HMGVRYIEVY KATGEEFVKI AGGTSLEVAR FLSREDQVIL
361 RLRGLPFSAG PTDVLGFLGP ECPVTGGTEG LLFVRHPDGR PTGDAFALFA CEELAQAALR
421 RHKGMLGKRY IELFRSTAAE VQQVLNRYAS GPLLPTLTAP LLPIPFPLAP GTGRDCVRLR
481 GLPYTATIED ILSFLGEAAA DIRPHGVHMV LNQQGRPSGD AFIQMTSAER ALAAAQRCHK
541 KVMKERYVEV VPCSTEEMSR VLMGGTLGRS GMSPPPCKLP CLSPPTYTTF QATPTLIPTE
601 TAALYPSSAL LPAARVPAAP TPVAYYPGPA TQLYLNYTAY YPSPPVSPTT VGYLTTPTAA
661 LASAPTSVLS QSGALVRMQG VPYTAGMKDL LSVFQAYQLP ADDYTSLMPV GDPPRTVLQA
721 PKEWVCLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ESRP2 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)
- 0.38
- Highest tissue expression
- 64 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 64 nTPM
- liver: 45 nTPM
- skin: 35 nTPM
- pancreas: 29 nTPM
- stomach: 26 nTPM
- vagina: 23 nTPM
Single-cell type
- esophageal apical cells: 142 nCPM
- late spermatids: 142 nCPM
- esophageal suprabasal cells: 100 nCPM
- syncytiotrophoblasts: 71 nCPM
- cytotrophoblasts: 47 nCPM
- esophageal basal cells: 38 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
- choroid plexus: 3.6 nTPM
- cerebellum: 3.1 nTPM
- cerebral cortex: 2.5 nTPM
- thalamus: 2.4 nTPM
- midbrain: 2.3 nTPM
- white matter: 2.3 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about ESRP2.
Disease | GeneticClinVar
2 pathogenic / likely-pathogenic of 145 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 0.72
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.82
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- selective
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
- alternative mRNA splicing, via spliceosome
- branching involved in salivary gland morphogenesis
- epithelial cell proliferation
- epithelial tube branching involved in lung morphogenesis
- positive regulation of epithelial cell proliferation
- regulation of RNA splicing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ESRP2 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 ESRP2 as an antibody target. Whether an autoantibody or antibody against ESRP2 could matter depends on whether native ESRP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ESRP2 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 ESRP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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