Homo sapiens Protein: SLC16A11
Summary
InnateDB Protein IDBP-23094.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC16A11
Protein Name solute carrier family 16, member 11 (monocarboxylic acid transporter 11)
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000310490
InnateDB Gene IDBG-23092 (SLC16A11)
Protein Structure
UniProt Annotation
Function Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates (By similarity). Probably involved in hepatic lipid metabolism: overexpression results in an increase of triacylglycerol(TAG) levels, small increases in intracellular diacylglycerols and decreases in lysophosphatidylcholine, cholesterol ester and sphingomyelin lipids. {ECO:0000250, ECO:0000269PubMed:24390345}.
Subcellular Localization Endoplasmic reticulum membrane {ECO:0000269PubMed:24390345}; Multi-pass membrane protein {ECO:0000269PubMed:24390345}.
Disease Associations Diabetes mellitus, non-insulin-dependent (NIDDM) [MIM:125853]: A multifactorial disorder of glucose homeostasis caused by a lack of sensitivity to the body's own insulin. Affected individuals usually have an obese body habitus and manifestations of a metabolic syndrome characterized by diabetes, insulin resistance, hypertension and hypertriglyceridemia. The disease results in long-term complications that affect the eyes, kidneys, nerves, and blood vessels. {ECO:0000269PubMed:24390345}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry. Variants Ile-113, Gly-127, Ser-340 and Thr-443 are individually associated with a 20% increased risk of NIDDM. These variants are present at 50% frequency in Native-American samples, 10% in east Asian, while they are rare in European and African samples populations. These haplotypes probably derive from H.sapiens neanderthalensis (Neanderthal) introgression (PubMed:24390345). {ECO:0000269PubMed:24390345}.
Tissue Specificity Expressed in liver, salivary gland and thyroid. {ECO:0000269PubMed:24390345}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0015293 symporter activity
Biological Process
GO:0006629 lipid metabolic process
GO:0055085 transmembrane transport
Cellular Component
GO:0005789 endoplasmic reticulum membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR011701 Major facilitator superfamily
IPR016196 Major facilitator superfamily domain, general substrate transporter
IPR020846 Major facilitator superfamily domain
PFAM PF07690
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8NCK7
PhosphoSite PhosphoSite-Q8NCK7
TrEMBL I3L431
UniProt Splice Variant
Entrez Gene 162515
UniGene Hs.336564
RefSeq NP_699188
HUGO HGNC:23093
OMIM 615765
CCDS CCDS11086
HPRD 11567
IMGT
EMBL AC040977 AK074674 BC093860 BC093886
GenPept AAH93860 AAH93886 BAC11128