RSC1A1
Regulatory solute carrier protein family 1 member 1
Also known as: RS1, RSCA1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q92681
- Gene
- RSC1A1
- Ensembl
- ENSG00000215695
- Chromosome
- 1
- Canonical length
- 617 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cell Junctions
OverviewNCBI Gene
The protein encoded by this intronless gene inhibits the expression of the solute carrier family 5 (sodium/glucose cotransporter), member 1 gene (SLC5A1) and downregulates exocytosis of the SLC5A1 protein. The encoded protein is sometimes found coating the trans-Golgi network and other times is localized to the nucleus, depending on the cell cycle stage. This protein also inhibits the expression of solute carrier family 22 (organic cation transporter), member 2 (SLC22A2). [provided by RefSeq, Dec 2015]
Canonical amino-acid sequenceUniProt
617 residues, UniProt reviewed canonical sequence.
>Q92681|RSC1A1
1 MSSLPTSDGF NHPARSSGQS PDVGNPMSLA RSVSASVCPI KPSDSDRIEP KAVKALKASA
61 EFQLNSEKKE HLSLQDLSDH ASSADHAPTD QSPAMPMQNS SEEITVAGNL EKSAERSTQG
121 LKFHLHTRQE ASLSVTSTRM HEPQMFLGEK DWHPENQNLS QVSDPQQHEE PGNEQYEVAQ
181 QKASHDQEYL CNIGDLELPE ERQQNQHKIV DLEATMKGNG LPQNVDPPSA KKSIPSSECS
241 GCSNSETFME IDTAQQSLVT LLNSTGRQNA NVKNIGALDL TLDNPLMEVE TSKCNPSSEI
301 LNDSISTQDL QPPETNVEIP GTNKEYGHYS SPSLCGSCQP SVESAEESCP SITAALKELH
361 ELLVVSSKPA SENTSEEVIC QSETIAEGQT SIKDLSERWT QNEHLTQNEQ CPQVSFHQAI
421 SVSVETEKLT GTSSDTGREA VENVNFRSLG DGLSTDKEGV PKSRESINKN RSVTVTSAKT
481 SNQLHCTLGV EISPKLLAGE EDALNQTSEQ TKSLSSNFIL VKDLGQGIQN SVTDRPETRE
541 NVCPDASRPL LEYEPPTSHP SSSPAILPPL IFPATDIDRI LRAGFTLQEA LGALHRVGGN
601 ADLALLVLLA KNIVVPTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RSC1A1 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.68
- Highest tissue expression
- 6.9 nTPM
Expression across tissuesHPA
Tissue
- liver: 6.9 nTPM
- bone marrow: 4.1 nTPM
- kidney: 3.8 nTPM
- esophagus: 3.7 nTPM
- tonsil: 3.1 nTPM
- smooth muscle: 3 nTPM
Single-cell type
- choroid plexus epithelial cells: 1.5 nCPM
- microglia: 1.3 nCPM
- oligodendrocytes: 0.8 nCPM
- ependymal cells: 0.7 nCPM
- brain excitatory neurons: 0.6 nCPM
- brain inhibitory neurons: 0.5 nCPM
Immune cell
- intermediate monocyte: 0.8 nTPM
- myeloid DC: 0.7 nTPM
- T-reg: 0.6 nTPM
- memory CD8 T-cell: 0.5 nTPM
- NK-cell: 0.4 nTPM
- total PBMC: 0.4 nTPM
Brain region
- white matter: 11 nTPM
- cerebral cortex: 8.5 nTPM
- choroid plexus: 8.4 nTPM
- medulla oblongata: 7.4 nTPM
- pons: 7.4 nTPM
- thalamus: 6.8 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)
- 1.52
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.24
- DepMap mean gene effect
- 0.01
- 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
- negative regulation of D-glucose transmembrane transport
- negative regulation of Golgi to plasma membrane protein transport
- negative regulation of protein localization to plasma membrane
- negative regulation of transport
- negative regulation of nucleoside transport
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RSC1A1 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 RSC1A1 as an antibody target. Whether an autoantibody or antibody against RSC1A1 could matter depends on whether native RSC1A1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RSC1A1 is annotated at the cell surface, where native RSC1A1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label RSC1A1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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