SNAPC5
snRNA-activating protein complex subunit 5
Also known as: SNAP19, SNPC5_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75971
- Gene
- SNAPC5
- Ensembl
- ENSG00000174446
- Chromosome
- 15
- Canonical length
- 98 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene encodes a subunit of the small nuclear RNA (snRNA)-activating protein complex that plays a role in the transcription of snRNA genes. This complex binds to the promoters of snRNA genes transcribed by either RNA polymerase II or III and recruits other regulatory factors to activate snRNA gene transcription. The encoded protein may play a role in stabilizing this complex. A pseudogene of this gene has been identified on chromosome 6. [provided by RefSeq, Jul 2016]
Canonical amino-acid sequenceUniProt
98 residues, UniProt reviewed canonical sequence.
>O75971|SNAPC5
1 MLSRLQELRK EEETLLRLKA ALHDQLNRLK VEELALQSMI SSRRGDEMLS SHTVPEQSHD
61 MLVHVDNEAS INQTTLELST KSHVTEEEEE EEEEESDSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SNAPC5 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)
- 0.59
- Highest tissue expression
- 43 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 43 nTPM
- skeletal muscle: 41 nTPM
- epididymis: 39 nTPM
- amygdala: 37 nTPM
- cerebral cortex: 36 nTPM
- heart muscle: 36 nTPM
Single-cell type
- late primary spermatocytes: 143 nCPM
- late spermatids: 129 nCPM
- early spermatids: 116 nCPM
- epididymal principal cells: 84 nCPM
- early primary spermatocytes: 80 nCPM
- hofbauer cells: 72 nCPM
Immune cell
- naive CD4 T-cell: 54 nTPM
- T-reg: 51 nTPM
- NK-cell: 49 nTPM
- non-classical monocyte: 47 nTPM
- naive CD8 T-cell: 45 nTPM
- memory CD8 T-cell: 45 nTPM
Brain region
- choroid plexus: 29 nTPM
- hypothalamus: 27 nTPM
- midbrain: 26 nTPM
- white matter: 25 nTPM
- cerebellum: 25 nTPM
- pons: 25 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)
- 1.89
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.72
- DepMap mean gene effect
- -1.22
- 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
- snRNA transcription by RNA polymerase II
- snRNA transcription by RNA polymerase III
- transcription initiation at RNA polymerase III promoter
Molecular functions
- RNA polymerase II general transcription initiation factor activity
- RNA polymerase III general transcription initiation factor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- snRNA-activating protein complex subunit 5
- snRNA-activating protein complex subunit 19, SNAPc subunit 19
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SNAPC5 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 SNAPC5 as an antibody target. Whether an autoantibody or antibody against SNAPC5 could matter depends on whether native SNAPC5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SNAPC5 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 SNAPC5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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