SLC7A6OS
Probable RNA polymerase II nuclear localization protein SLC7A6OS
Also known as: FLJ13291, Iwr1, S7A6O_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96CW6
- Gene
- SLC7A6OS
- Ensembl
- ENSG00000103061
- Chromosome
- 16
- Canonical length
- 309 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Predicted to be involved in developmental process. Predicted to act upstream of or within hematopoietic progenitor cell differentiation. Predicted to be located in cytoplasm and nucleus. Implicated in progressive myoclonus epilepsy. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
309 residues, UniProt reviewed canonical sequence.
>Q96CW6|SLC7A6OS
1 MEAARTAVLR VKRKRSAEPA EALVLACKRL RSDAVESAAQ KTSEGLERAA ENNVFHLVAT
61 VCSQEEPVQP LLREVLRPSR DSQQRVRRNL RASAREVRQE GRYRVLSSRR SLGTTSSGQE
121 SEYTPGNPEA AGNSGFQLLD LVHEEGEPEA ASAGSCKTSD PDVILCNSVE LIRERLTVSE
181 DGPGVRRQEE QKHDDYVYDI YYLETATPGW IENILSVQPY SQEWELVNDD QEPEDIYDDE
241 DDENSENNWR NEYPEEESSD GDEDSRGSAD YNSLSEEERG SSRQRMWSKY PLDVQKEFGY
301 DSPHDLDSDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC7A6OS 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)
- 0.54
- Highest tissue expression
- 17 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 17 nTPM
- lymph node: 15 nTPM
- adipose tissue: 14 nTPM
- bone marrow: 13 nTPM
- heart muscle: 13 nTPM
- spleen: 13 nTPM
Single-cell type
- cardiomyocytes: 636 nCPM
- adipocytes: 320 nCPM
- thymic myoid cells: 280 nCPM
- myonuclei: 156 nCPM
- epicardial cells: 73 nCPM
- fibro-adipogenic progenitors: 49 nCPM
Immune cell
- basophil: 29 nTPM
- eosinophil: 26 nTPM
- MAIT T-cell: 17 nTPM
- T-reg: 16 nTPM
- naive CD4 T-cell: 16 nTPM
- naive B-cell: 15 nTPM
Brain region
- white matter: 20 nTPM
- cerebellum: 18 nTPM
- medulla oblongata: 17 nTPM
- basal ganglia: 17 nTPM
- pons: 17 nTPM
- midbrain: 16 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about SLC7A6OS.
Disease | AllUniProt
Conditions SLC7A6OS is implicated in, by any mechanism.
- Epilepsy, progressive myoclonic 12 (EPM12) MIM:619191
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)
- 0.61
- gnomAD pLI
- 0.17
- gnomAD missense Z
- 0.18
- DepMap mean gene effect
- -1.02
- DepMap dependency class
- common
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
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Transcription factor Iwr1 domain
- Probable RNA polymerase II nuclear localization protein SLC7A6OS
- Transcription factor Iwr1
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC7A6OS as an antibody target. Whether an autoantibody or antibody against SLC7A6OS could matter depends on whether native SLC7A6OS is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC7A6OS 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 SLC7A6OS as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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