SLC16A6
Monocarboxylate transporter 7
Also known as: MCT6, MCT7, MOT7_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O15403
- Gene
- SLC16A6
- Ensembl
- ENSG00000108932
- Chromosome
- 17
- Canonical length
- 523 aa
- Protein class
- Metabolic proteins, Plasma proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Vesicles
OverviewNCBI Gene
Predicted to enable monocarboxylic acid transmembrane transporter activity. Predicted to be involved in monocarboxylic acid transport. Predicted to be located in basolateral plasma membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
523 residues, UniProt reviewed canonical sequence.
>O15403|SLC16A6
1 MTQNKLKLCS KANVYTEVPD GGWGWAVAVS FFFVEVFTYG IIKTFGVFFN DLMDSFNESN
61 SRISWIISIC VFVLTFSAPL ATVLSNRFGH RLVVMLGGLL VSTGMVAASF SQEVSHMYVA
121 IGIISGLGYC FSFLPTVTIL SQYFGKRRSI VTAVASTGEC FAVFAFAPAI MALKERIGWR
181 YSLLFVGLLQ LNIVIFGALL RPIFIRGPAS PKIVIQENRK EAQYMLENEK TRTSIDSIDS
241 GVELTTSPKN VPTHTNLELE PKADMQQVLV KTSPRPSEKK APLLDFSILK EKSFICYALF
301 GLFATLGFFA PSLYIIPLGI SLGIDQDRAA FLLSTMAIAE VFGRIGAGFV LNREPIRKIY
361 IELICVILLT VSLFAFTFAT EFWGLMSCSI FFGFMVGTIG GTHIPLLAED DVVGIEKMSS
421 AAGVYIFIQS IAGLAGPPLA GLLVDQSKIY SRAFYSCAAG MALAAVCLAL VRPCKMGLCQ
481 HHHSGETKVV SHRGKTLQDI PEDFLEMDLA KNEHRVHVQM EPVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC16A6 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)
- 0.32
- Highest tissue expression
- 43 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 43 nTPM
- epididymis: 31 nTPM
- retina: 28 nTPM
- esophagus: 10 nTPM
- bone marrow: 9.2 nTPM
- appendix: 6.8 nTPM
Single-cell type
- monocytes: 276 nCPM
- choroid plexus epithelial cells: 168 nCPM
- neutrophils: 159 nCPM
- endometrial glandular cells: 101 nCPM
- epididymal principal cells: 93 nCPM
- rod photoreceptor cells: 60 nCPM
Immune cell
- neutrophil: 4.5 nTPM
- classical monocyte: 2.5 nTPM
- intermediate monocyte: 2.3 nTPM
- gdT-cell: 1.6 nTPM
- myeloid DC: 1.5 nTPM
- T-reg: 1.3 nTPM
Brain region
- choroid plexus: 108 nTPM
- thalamus: 16 nTPM
- hypothalamus: 16 nTPM
- pons: 16 nTPM
- hippocampal formation: 15 nTPM
- basal ganglia: 14 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)
- 0.84
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.84
- DepMap mean gene effect
- -0.21
- DepMap dependency class
- selective
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SLC16A6 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 SLC16A6 as an antibody target. Whether an autoantibody or antibody against SLC16A6 could matter depends on whether native SLC16A6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC16A6 is annotated at the cell surface, where native SLC16A6 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 SLC16A6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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