SNAPC2
snRNA-activating protein complex subunit 2
Also known as: PTFdelta, SNAP45, SNPC2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q13487
- Gene
- SNAPC2
- Ensembl
- ENSG00000104976
- Chromosome
- 19
- Canonical length
- 334 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies,Cytosol
OverviewNCBI Gene
This gene encodes a subunit of the snRNA-activating protein complex which is associated with the TATA box-binding protein. The encoded protein is necessary for RNA polymerase II and III dependent small-nuclear RNA gene transcription. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009]
Canonical amino-acid sequenceUniProt
334 residues, UniProt reviewed canonical sequence.
>Q13487|SNAPC2
1 MKPPPRRRAA PARYLGEVTG PATWSAREKR QLVRLLQARQ GQPEPDATEL ARELRGRSEA
61 EIRVFLQQLK GRVAREAIQK VHPGGLQGPR RREAQPPAPI EVWTDLAEKI TGPLEEALAV
121 AFSQVLTIAA TEPVTLLHSK PPKPTQARGK PLLLSAPGGQ EDPAPEIPSS APAAPSSAPR
181 TPDPAPEKPS ESSAGPSTEE DFAVDFEKIY KYLSSVSRSG RSPELSAAES AVVLDLLMSL
241 PEELPLLPCT ALVEHMTETY LRLTAPQPIP AGGSLGPAAE GDGAGSKAPE ETPPATEKAE
301 HSELKSPWQA AGICPLNPFL VPLELLGRAA TPARLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SNAPC2 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)
- 0.56
- Highest tissue expression
- 51 nTPM
Expression across tissuesHPA
Tissue
- endometrium: 51 nTPM
- cervix: 38 nTPM
- blood vessel: 37 nTPM
- fallopian tube: 36 nTPM
- colon: 35 nTPM
- testis: 32 nTPM
Single-cell type
- decidual stromal cells: 87 nCPM
- oocytes: 65 nCPM
- undifferentiated spermatogonia: 48 nCPM
- smooth muscle cells: 47 nCPM
- breast secretory cells: 38 nCPM
- megakaryocytes: 37 nCPM
Immune cell
- non-classical monocyte: 34 nTPM
- intermediate monocyte: 31 nTPM
- myeloid DC: 30 nTPM
- NK-cell: 28 nTPM
- T-reg: 24 nTPM
- classical monocyte: 24 nTPM
Brain region
- cerebral cortex: 30 nTPM
- basal ganglia: 22 nTPM
- hippocampal formation: 21 nTPM
- pons: 20 nTPM
- hypothalamus: 19 nTPM
- medulla oblongata: 18 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)
- 0.86
- gnomAD pLI
- 0.1
- gnomAD missense Z
- -1.46
- DepMap mean gene effect
- -1.29
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Small nuclear RNA activating complex subunit 2
- Small nuclear RNA activating complex (SNAPc), subunit 2
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SNAPC2 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 SNAPC2 as an antibody target. Whether an autoantibody or antibody against SNAPC2 could matter depends on whether native SNAPC2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SNAPC2 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 SNAPC2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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