SRSF12
Serine/arginine-rich splicing factor 12
Also known as: SFRS13B, SFRS19, SRrp35, SRS12_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8WXF0
- Gene
- SRSF12
- Ensembl
- ENSG00000154548
- Chromosome
- 6
- Canonical length
- 261 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Enables RNA binding activity. Involved in mRNA 5'-splice site recognition and regulation of alternative mRNA splicing, via spliceosome. Predicted to be located in nucleoplasm. Predicted to be active in nuclear speck. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
261 residues, UniProt reviewed canonical sequence.
>Q8WXF0|SRSF12
1 MSRYTRPPNT SLFIRNVADA TRPEDLRREF GRYGPIVDVY IPLDFYTRRP RGFAYVQFED
61 VRDAEDALYN LNRKWVCGRQ IEIQFAQGDR KTPGQMKSKE RHPCSPSDHR RSRSPSQRRT
121 RSRSSSWGRN RRRSDSLKES RHRRFSYSQS KSRSKSLPRR STSARQSRTP RRNFGSRGRS
181 RSKSLQKRSK SIGKSQSSSP QKQTSSGTKS RSHGRHSDSI ARSPCKSPKG YTNSETKVQT
241 AKHSHFRSHS RSRSYRHKNS WLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SRSF12 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)
- 0.58
- Highest tissue expression
- 11 nTPM
Expression across tissuesHPA
Tissue
- testis: 11 nTPM
- cerebral cortex: 4.1 nTPM
- hypothalamus: 3.8 nTPM
- amygdala: 3.6 nTPM
- basal ganglia: 3.2 nTPM
- cerebellum: 3.2 nTPM
Single-cell type
- late spermatids: 332 nCPM
- epicardial cells: 307 nCPM
- late primary spermatocytes: 188 nCPM
- early spermatids: 155 nCPM
- undifferentiated spermatogonia: 69 nCPM
- differentiating spermatogonia: 65 nCPM
Immune cell
- NK-cell: 0.5 nTPM
- basophil: 0.2 nTPM
- gdT-cell: 0.1 nTPM
- MAIT T-cell: 0.1 nTPM
- memory CD4 T-cell: 0.1 nTPM
- naive B-cell: 0.1 nTPM
Brain region
- hypothalamus: 11 nTPM
- cerebellum: 11 nTPM
- basal ganglia: 9.4 nTPM
- cerebral cortex: 9.4 nTPM
- hippocampal formation: 8.3 nTPM
- midbrain: 7.6 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)
- 0.72
- gnomAD pLI
- 0.03
- gnomAD missense Z
- 1.11
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
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 5'-splice site recognition
- negative regulation of mRNA splicing, via spliceosome
- regulation of alternative mRNA splicing, via spliceosome
- spliceosomal tri-snRNP complex assembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SRSF12 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 SRSF12 as an antibody target. Whether an autoantibody or antibody against SRSF12 could matter depends on whether native SRSF12 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SRSF12 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 SRSF12 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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