SNRNP40
U5 small nuclear ribonucleoprotein 40 kDa protein
Also known as: HPRP8BP, PRP8BP, PRPF8BP, SNR40_HUMAN, SPF38, WDR57
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96DI7
- Gene
- SNRNP40
- Ensembl
- ENSG00000060688
- Chromosome
- 1
- Canonical length
- 357 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nuclear speckles
OverviewNCBI Gene
This gene encodes a component of the U5 small nuclear ribonucleoprotein (snRNP) particle. The U5 snRNP is part of the spliceosome, a multiprotein complex that catalyzes the removal of introns from pre-messenger RNAs. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
357 residues, UniProt reviewed canonical sequence.
>Q96DI7|SNRNP40
1 MIEQQKRKGP ELPLVPVKRQ RHELLLGAGS GPGAGQQQAT PGALLQAGPP RCSSLQAPIM
61 LLSGHEGEVY CCKFHPNGST LASAGFDRLI LLWNVYGDCD NYATLKGHSG AVMELHYNTD
121 GSMLFSASTD KTVAVWDSET GERVKRLKGH TSFVNSCYPA RRGPQLVCTG SDDGTVKLWD
181 IRKKAAIQTF QNTYQVLAVT FNDTSDQIIS GGIDNDIKVW DLRQNKLTYT MRGHADSVTG
241 LSLSSEGSYL LSNAMDNTVR VWDVRPFAPK ERCVKIFQGN VHNFEKNLLR CSWSPDGSKI
301 AAGSADRFVY VWDTTSRRIL YKLPGHAGSI NEVAFHPDEP IIISASSDKR LYMGEIQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SNRNP40 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)
- 0.29
- Highest tissue expression
- 38 nTPM
Expression across tissuesHPA
Tissue
- tonsil: 38 nTPM
- thymus: 38 nTPM
- lymph node: 33 nTPM
- bone marrow: 28 nTPM
- urinary bladder: 22 nTPM
- ovary: 22 nTPM
Single-cell type
- early primary spermatocytes: 165 nCPM
- cytotrophoblasts: 137 nCPM
- migrating cytotrophoblasts: 124 nCPM
- megakaryocytes: 111 nCPM
- extravillous trophoblasts: 106 nCPM
- erythrocyte progenitors: 101 nCPM
Immune cell
- total PBMC: 161 nTPM
- naive CD8 T-cell: 116 nTPM
- MAIT T-cell: 113 nTPM
- NK-cell: 111 nTPM
- T-reg: 111 nTPM
- basophil: 103 nTPM
Brain region
- white matter: 38 nTPM
- cerebellum: 30 nTPM
- pons: 30 nTPM
- medulla oblongata: 29 nTPM
- basal ganglia: 27 nTPM
- spinal cord: 26 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)
- 0.4
- gnomAD pLI
- 0.85
- gnomAD missense Z
- 1.55
- DepMap mean gene effect
- -0.72
- 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
- mRNA splicing, via spliceosome
- RNA processing
- RNA splicing
- RNA splicing, via transesterification reactions
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SNRNP40 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 SNRNP40 as an antibody target. Whether an autoantibody or antibody against SNRNP40 could matter depends on whether native SNRNP40 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SNRNP40 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 SNRNP40 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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