SNRNP27
U4/U6.U5 small nuclear ribonucleoprotein 27 kDa protein
Also known as: RY1, SNR27_HUMAN, U4/U6.U5-27K
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8WVK2
- Gene
- SNRNP27
- Ensembl
- ENSG00000124380
- Chromosome
- 2
- Canonical length
- 155 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene encodes a serine/arginine-rich (SR) protein. SR proteins play important roles in pre-mRNA splicing by facilitating the recognition and selection of splice sites. The encoded protein associates with the 25S U4/U6.U5 tri-snRNP, a major component of the U2-type spiceosome. The expression of this gene may be altered in cells infected with the human T-cell lymphotropic virus type 1 (HTLV-1) retrovirus. A pseudogene of this gene is located on the long arm of chromosome 5. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Feb 2011]
Canonical amino-acid sequenceUniProt
155 residues, UniProt reviewed canonical sequence.
>Q8WVK2|SNRNP27
1 MGRSRSRSPR RERRRSRSTS RERERRRRER SRSRERDRRR SRSRSPHRRR SRSPRRHRST
61 SPSPSRLKER RDEEKKETKE TKSKERQITE EDLEGKTEEE IEMMKLMGFA SFDSTKGKKV
121 DGSVNAYAIN VSQKRKYRQY MNRKGGFNRP LDFIALocalizationUniProt · AlphaFold · HPA
Whether an antibody against SNRNP27 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)
- 0.68
- Highest tissue expression
- 67 nTPM
Expression across tissuesHPA
Tissue
- tongue: 67 nTPM
- skeletal muscle: 58 nTPM
- bone marrow: 41 nTPM
- heart muscle: 37 nTPM
- spinal cord: 37 nTPM
- amygdala: 34 nTPM
Single-cell type
- tuft cells: 161 nCPM
- megakaryocytes: 80 nCPM
- hepatocytes: 64 nCPM
- parietal cells: 60 nCPM
- early primary spermatocytes: 51 nCPM
- late primary spermatocytes: 49 nCPM
Immune cell
- basophil: 43 nTPM
- plasmacytoid DC: 41 nTPM
- eosinophil: 39 nTPM
- memory B-cell: 38 nTPM
- naive B-cell: 32 nTPM
- NK-cell: 32 nTPM
Brain region
- white matter: 42 nTPM
- cerebral cortex: 39 nTPM
- cerebellum: 37 nTPM
- hypothalamus: 37 nTPM
- midbrain: 35 nTPM
- basal ganglia: 34 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)
- 1.01
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.76
- DepMap mean gene effect
- -1.08
- DepMap dependency class
- common
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
- via spliceosome
- mRNA splicing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- U4/U6.U5 small nuclear ribonucleoprotein 27kDa protein
- U4/U6.U5 small nuclear ribonucleoproteins
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SNRNP27 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 SNRNP27 as an antibody target. Whether an autoantibody or antibody against SNRNP27 could matter depends on whether native SNRNP27 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SNRNP27 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 SNRNP27 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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