SLC2A4RG
SLC2A4 regulator
Also known as: GEF, HDBP1, S2A4R_HUMAN, Si-1-2, Si-1-2-19
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NR83
- Gene
- SLC2A4RG
- Ensembl
- ENSG00000125520
- Chromosome
- 20
- Canonical length
- 387 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nuclear speckles
OverviewNCBI Gene
The protein encoded by this gene is a nuclear transcription factor involved in the activation of the solute carrier family 2 member 4 gene. The encoded protein interacts with another transcription factor, myocyte enhancer factor 2, to activate transcription of this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
387 residues, UniProt reviewed canonical sequence.
>Q9NR83|SLC2A4RG
1 MERPPPRAAG RDPSALRAEA PWLRAEGPGP RAAPVTVPTP PQGSSVGGGF AGLEFARPQE
61 SEPRASDLGA PRTWTGAAAG PRTPSAHIPV PAQRATPGKA RLDEVMAAAA LTSLSTSPLL
121 LGAPVAAFSP EPGLEPWKEA LVRPPGSYSS SSNSGDWGWD LASDQSSPST PSPPLPPEAA
181 HFLFGEPTLR KRKSPAQVMF QCLWKSCGKV LSTASAMQRH IRLVHLGRQA EPEQSDGEED
241 FYYTELDVGV DTLTDGLSSL TPVSPTASMP PAFPRLELPE LLEPPALPSP LRPPAPPLPP
301 PPVLSTVANP QSCHSDRVYQ GCLTPARLEP QPTEVGACPP ALSSRIGVTL RKPRGDAKKC
361 RKVYGMERRD LWCTACRWKK ACQRFLDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC2A4RG 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)
- 0.64
- Highest tissue expression
- 86 nTPM
Expression across tissuesHPA
Tissue
- liver: 86 nTPM
- kidney: 45 nTPM
- skeletal muscle: 44 nTPM
- heart muscle: 36 nTPM
- adipose tissue: 30 nTPM
- blood vessel: 28 nTPM
Single-cell type
- hepatocytes: 142 nCPM
- breast myoepithelial cells: 104 nCPM
- breast lactating cells: 100 nCPM
- smooth muscle cells: 85 nCPM
- erythrocyte progenitors: 77 nCPM
- sertoli cells: 68 nCPM
Immune cell
- T-reg: 1.1 nTPM
- gdT-cell: 0.9 nTPM
- memory CD4 T-cell: 0.9 nTPM
- naive CD4 T-cell: 0.7 nTPM
- naive CD8 T-cell: 0.7 nTPM
- memory CD8 T-cell: 0.5 nTPM
Brain region
- spinal cord: 11 nTPM
- amygdala: 11 nTPM
- basal ganglia: 11 nTPM
- white matter: 11 nTPM
- medulla oblongata: 10 nTPM
- hypothalamus: 10 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)
- 0.68
- gnomAD pLI
- 0.22
- gnomAD missense Z
- 0.19
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 10% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- DNA-binding transcription factor activity
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SLC2A4RG 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 SLC2A4RG as an antibody target. Whether an autoantibody or antibody against SLC2A4RG could matter depends on whether native SLC2A4RG is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC2A4RG 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 SLC2A4RG as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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