SLC2A6
Solute carrier family 2, facilitated glucose transporter member 6
Also known as: GLUT6, GLUT9, GTR6_HUMAN, HSA011372
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UGQ3
- Gene
- SLC2A6
- Ensembl
- ENSG00000160326
- Chromosome
- 9
- Canonical length
- 507 aa
- Protein class
- Metabolic proteins, Predicted membrane proteins, Transporters
OverviewNCBI Gene
Hexose transport into mammalian cells is catalyzed by a family of membrane proteins, including SLC2A6, that contain 12 transmembrane domains and a number of critical conserved residues.[supplied by OMIM, Jul 2002]
Canonical amino-acid sequenceUniProt
507 residues, UniProt reviewed canonical sequence.
>Q9UGQ3|SLC2A6
1 MQEPLLGAEG PDYDTFPEKP PPSPGDRARV GTLQNKRVFL ATFAAVLGNF SFGYALVYTS
61 PVIPALERSL DPDLHLTKSQ ASWFGSVFTL GAAAGGLSAM ILNDLLGRKL SIMFSAVPSA
121 AGYALMAGAH GLWMLLLGRT LTGFAGGLTA ACIPVYVSEI APPGVRGALG ATPQLMAVFG
181 SLSLYALGLL LPWRWLAVAG EAPVLIMILL LSFMPNSPRF LLSRGRDEEA LRALAWLRGT
241 DVDVHWEFEQ IQDNVRRQSS RVSWAEARAP HVCRPITVAL LMRLLQQLTG ITPILVYLQS
301 IFDSTAVLLP PKDDAAIVGA VRLLSVLIAA LTMDLAGRKV LLFVSAAIMF AANLTLGLYI
361 HFGPRPLSPN STAGLESESW GDLAQPLAAP AGYLTLVPLL ATMLFIMGYA VGWGPITWLL
421 MSEVLPLRAR GVASGLCVLA SWLTAFVLTK SFLPVVSTFG LQVPFFFFAA ICLVSLVFTG
481 CCVPETKGRS LEQIESFFRT GRRSFLRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC2A6 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 12
- Mean surface accessibility (rSASA)
- 0.26
- Highest tissue expression
- 18 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 18 nTPM
- hypothalamus: 14 nTPM
- spleen: 14 nTPM
- midbrain: 13 nTPM
- hippocampal formation: 11 nTPM
- cerebellum: 10 nTPM
Single-cell type
- other brain neurons: 25 nCPM
- brain excitatory neurons: 19 nCPM
- brain inhibitory neurons: 16 nCPM
- astrocytes: 9.7 nCPM
- oligodendrocyte progenitor cells: 7.2 nCPM
- oligodendrocytes: 6.8 nCPM
Immune cell
- non-classical monocyte: 74 nTPM
- basophil: 46 nTPM
- intermediate monocyte: 37 nTPM
- classical monocyte: 18 nTPM
- plasmacytoid DC: 17 nTPM
- myeloid DC: 16 nTPM
Brain region
- pons: 26 nTPM
- cerebral cortex: 20 nTPM
- medulla oblongata: 19 nTPM
- thalamus: 18 nTPM
- hypothalamus: 17 nTPM
- midbrain: 16 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)
- 0.99
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.81
- DepMap mean gene effect
- 0
- DepMap dependency class
- selective
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
- D-glucose transmembrane transport
- dehydroascorbic acid transport
- fructose transmembrane transport
- hexose transmembrane transport
- regulation of glycolytic process
- transmembrane transport
Molecular functions
- D-glucose transmembrane transporter activity
- dehydroascorbic acid transmembrane transporter activity
- fructose transmembrane transporter activity
- transmembrane transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC2A6 as an antibody target. Whether an autoantibody or antibody against SLC2A6 could matter depends on whether native SLC2A6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC2A6 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 SLC2A6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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