SREK1
Splicing regulatory glutamine/lysine-rich protein 1
Also known as: DKFZp564B176, SFRS12, SREK1_HUMAN, SRrp508, SRrp86
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8WXA9
- Gene
- SREK1
- Ensembl
- ENSG00000153914
- Chromosome
- 5
- Canonical length
- 508 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear speckles
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a member of a family of serine/arginine-rich (SR) splicing proteins containing RNA recognition motif (RRM) domains. The encoded protein interacts with other SR proteins to modulate splice site selection. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]
Canonical amino-acid sequenceUniProt
508 residues, UniProt reviewed canonical sequence.
>Q8WXA9|SREK1
1 MTSLMPGAGL LPIPTPNPLT TLGVSLSSLG AIPAAALDPN IATLGEIPQP PLMGNVDPSK
61 IDEIRRTVYV GNLNSQTTTA DQLLEFFKQV GEVKFVRMAG DETQPTRFAF VEFADQNSVP
121 RALAFNGVMF GDRPLKINHS NNAIVKPPEM TPQAAAKELE EVMKRVREAQ SFISAAIEPE
181 SGKSNERKGG RSRSHTRSKS RSSSKSHSRR KRSQSKHRSR SHNRSRSRQK DRRRSKSPHK
241 KRSKSRERRK SRSRSHSRDK RKDTREKIKE KERVKEKDRE KEREREKERE KEKERGKNKD
301 RDKEREKDRE KDKEKDRERE REKEHEKDRD KEKEKEQDKE KEREKDRSKE IDEKRKKDKK
361 SRTPPRSYNA SRRSRSSSRE RRRRRSRSSS RSPRTSKTIK RKSSRSPSPR SRNKKDKKRE
421 KERDHISERR ERERSTSMRK SSNDRDGKEK LEKNSTSLKE KEHNKEPDSS VSKEVDDKDA
481 PRTEENKIQH NGNCQLNEEN LSTKTEAVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SREK1 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
- 19 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 19 nTPM
- cerebellum: 11 nTPM
- retina: 8.8 nTPM
- pancreas: 8.7 nTPM
- endometrium: 8.5 nTPM
- skin: 8.5 nTPM
Single-cell type
- somatotrophs: 201 nCPM
- thyrotrophs: 187 nCPM
- neutrophil progenitors: 186 nCPM
- lactotrophs: 175 nCPM
- pituicytes/fscs: 171 nCPM
- sertoli cells: 166 nCPM
Immune cell
- basophil: 4.9 nTPM
- naive B-cell: 3.8 nTPM
- NK-cell: 3.8 nTPM
- memory B-cell: 3.2 nTPM
- plasmacytoid DC: 3.1 nTPM
- eosinophil: 2.8 nTPM
Brain region
- choroid plexus: 22 nTPM
- cerebellum: 18 nTPM
- cerebral cortex: 16 nTPM
- white matter: 16 nTPM
- hypothalamus: 16 nTPM
- basal ganglia: 15 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)
- 0.35
- gnomAD pLI
- 0.91
- gnomAD missense Z
- 2.26
- DepMap mean gene effect
- -0.25
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% 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
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SREK1 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 SREK1 as an antibody target. Whether an autoantibody or antibody against SREK1 could matter depends on whether native SREK1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SREK1 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 SREK1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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