SLC2A14
Solute carrier family 2, facilitated glucose transporter member 14
Also known as: GLUT14, GTR14_HUMAN, SLC2A3P3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TDB8
- Gene
- SLC2A14
- Ensembl
- ENSG00000173262
- Chromosome
- 12
- Canonical length
- 520 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Plasma membrane
OverviewNCBI Gene
Members of the glucose transporter (GLUT) family, including SLC2A14, are highly conserved integral membrane proteins that transport hexoses such as glucose and fructose into all mammalian cells. GLUTs show tissue and cell-type specific expression (Wu and Freeze, 2002 [PubMed 12504846]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
520 residues, UniProt reviewed canonical sequence.
>Q8TDB8|SLC2A14
1 MEFHNGGHVS GIGGFLVSLT SRMKPHTLAV TPALIFAITV ATIGSFQFGY NTGVINAPET
61 IIKEFINKTL TDKANAPPSE VLLTNLWSLS VAIFSVGGMI GSFSVGLFVN RFGRRNSMLI
121 VNLLAATGGC LMGLCKIAES VEMLILGRLV IGLFCGLCTG FVPMYIGEIS PTALRGAFGT
181 LNQLGIVIGI LVAQIFGLEL ILGSEELWPV LLGFTILPAI LQSAALPCCP ESPRFLLINR
241 KKEENATRIL QRLWGTQDVS QDIQEMKDES ARMSQEKQVT VLELFRVSSY RQPIIISIVL
301 QLSQQLSGIN AVFYYSTGIF KDAGVQQPIY ATISAGVVNT IFTLLSLFLV ERAGRRTLHM
361 IGLGGMAFCS TLMTVSLLLK NHYNGMSFVC IGAILVFVAC FEIGPGPIPW FIVAELFSQG
421 PRPAAMAVAG CSNWTSNFLV GLLFPSAAYY LGAYVFIIFT GFLITFLAFT FFKVPETRGR
481 TFEDITRAFE GQAHGADRSG KDGVMGMNSI EPAKETTTNVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC2A14 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
- 12
- Mean surface accessibility (rSASA)
- 0.24
- Highest tissue expression
- 76 nTPM
Expression across tissuesHPA
Tissue
- testis: 76 nTPM
- pancreas: 6.2 nTPM
- bone marrow: 5.9 nTPM
- adrenal gland: 5.1 nTPM
- liver: 2.6 nTPM
- ovary: 2.6 nTPM
Single-cell type
- pancreatic acinar cells: 109 nCPM
- late primary spermatocytes: 103 nCPM
- adrenal cortex cells: 89 nCPM
- early primary spermatocytes: 64 nCPM
- granulosa cells: 62 nCPM
- erythrocyte progenitors: 46 nCPM
Immune cell
- basophil: 3.7 nTPM
- neutrophil: 3.3 nTPM
- eosinophil: 1 nTPM
- T-reg: 1 nTPM
- NK-cell: 0.7 nTPM
- MAIT T-cell: 0.6 nTPM
Brain region
- cerebellum: 16 nTPM
- choroid plexus: 10 nTPM
- hippocampal formation: 9.3 nTPM
- hypothalamus: 9 nTPM
- cerebral cortex: 8.3 nTPM
- basal ganglia: 7.4 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)
- 0.6
- gnomAD pLI
- 0.04
- gnomAD missense Z
- 1.32
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell differentiation
- D-glucose import
- D-glucose transmembrane transport
- dehydroascorbic acid transport
- spermatogenesis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC2A14 as an antibody target. Whether an autoantibody or antibody against SLC2A14 could matter depends on whether native SLC2A14 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC2A14 is annotated at the cell surface, where native SLC2A14 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 SLC2A14 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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