Gene Gene information from NCBI Gene database.
Entrez ID 162515
Gene name Solute carrier family 16 member 11
Gene symbol SLC16A11
Synonyms (NCBI Gene)
MCT 11MCT11
Chromosome 17
Chromosome location 17p13.1
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 28666119
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005789 Component Endoplasmic reticulum membrane IDA 24390345
GO:0005789 Component Endoplasmic reticulum membrane IEA
GO:0005886 Component Plasma membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
615765 23093 ENSG00000174326
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NCK7
Protein name Monocarboxylate transporter 11 (MCT 11) (Solute carrier family 16 member 11)
Protein function Proton-linked monocarboxylate transporter. It catalyzes the transport of pyruvate across the plasma membrane (PubMed:28666119). Probably involved in hepatic lipid metabolism: overexpression results in an increase of triacylglycerol(TAG) levels,
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07690 MFS_1 41 321 Major Facilitator Superfamily Family
Tissue specificity TISSUE SPECIFICITY: Expressed in liver, salivary gland and thyroid. {ECO:0000269|PubMed:24390345}.
Sequence
MPAPQRKHRRGGFSHRCFPTPQTAMTPQPAGPPDGGWGWVVAAAAFAINGLSYGLLRSLG
LAFPDLAEHFDRSAQDTAWISALALAVQQAASPVGSALSTRWGARPVVMVGGVLASLGFV
FSAFASDLLHLYLGLGLLAGFGWALVFAPALGTLSRYFSRRRVLAVGLALTGNGASSLLL
APALQLLLDTFGWRGALLLLGAITLHLTPCGALLLPLVLPGDPPAPPRSPLAALGLSLFT
RRAFSIFALGTALVGGGYFVPYVHLAPHALDRGLGGYGAALVVAVAAMGDAGARLVCGWL
ADQGWVPLPRLLAVFGALTGL
GLWVVGLVPVVGGEESWGGPLLAAAVAYGLSAGSYAPLV
FGVLPGLVGVGGVVQATGLVMMLMSLGGLLGPPLSGFLRDETGDFTASFLLSGSLILSGS
FIYIGLPRALPSCGPASPPATPPPETGELLPAPQAVLLSPGGPGSTLDTTC
Sequence length 471
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
CROHN'S DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DIABETIC KETOACIDOSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INFLAMMATORY BOWEL DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinoma Hepatocellular Associate 37077914
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Associate 26487785, 30696834, 32699108, 33479058
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Diabetes Mellitus Type 1 Associate 38530923
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Type 2 Associate 25973943, 26487785, 27175665, 28666119, 30696834, 33479058, 33909378, 38530923
★☆☆☆☆
Found in Text Mining only
Obesity Associate 26487785, 32699108, 33909378
★☆☆☆☆
Found in Text Mining only
Ovarian Neoplasms Associate 23571109
★☆☆☆☆
Found in Text Mining only