Homo sapiens Protein: SLC2A10 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-79450.5 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | SLC2A10 | ||||||||||||||||||
Protein Name | solute carrier family 2 (facilitated glucose transporter), member 10 | ||||||||||||||||||
Synonyms | |||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000352216 | ||||||||||||||||||
InnateDB Gene | IDBG-79448 (SLC2A10) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | Facilitative glucose transporter. | ||||||||||||||||||
Subcellular Localization | Endomembrane system {ECO:0000269PubMed:16550171}; Multi-pass membrane protein {ECO:0000269PubMed:16550171}. Cytoplasm, perinuclear region {ECO:0000269PubMed:16550171}. | ||||||||||||||||||
Disease Associations | Arterial tortuosity syndrome (ATS) [MIM:208050]: An autosomal recessive disorder characterized by tortuosity and elongation of major arteries, often resulting in death at young age. Other typical features include aneurysms of large arteries and stenosis of the pulmonary artery, in association with facial features and several connective tissue manifestations such as soft skin and joint laxity. Histopathological findings include fragmentation of elastic fibers in the tunica media of large arteries. {ECO:0000269PubMed:16550171, ECO:0000269PubMed:17935213}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | Widely expressed; highest levels in liver and pancreas. {ECO:0000269PubMed:11592815}. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR003663
Sugar/inositol transporter IPR005828 General substrate transporter IPR011701 Major facilitator superfamily IPR016196 Major facilitator superfamily domain, general substrate transporter IPR020846 Major facilitator superfamily domain |
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PFAM |
PF00083
PF07690 |
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PRINTS |
PR00171
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PIRSF | |||||||||||||||||||
SMART | |||||||||||||||||||
TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | O95528 | ||||||||||||||||||
PhosphoSite | PhosphoSite-O95528 | ||||||||||||||||||
TrEMBL | Q8TDC7 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 81031 | ||||||||||||||||||
UniGene | Hs.597410 | ||||||||||||||||||
RefSeq | NP_110404 | ||||||||||||||||||
HUGO | HGNC:13444 | ||||||||||||||||||
OMIM | 606145 | ||||||||||||||||||
CCDS | CCDS13402 | ||||||||||||||||||
HPRD | 05851 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AF248053 AF321240 AF479407 AK290961 AL031055 AL137188 BC101657 BC113423 CH471077 | ||||||||||||||||||
GenPept | AAI01658 AAI13424 AAK26294 AAK31911 AAL87106 BAF83650 CAA19926 CAB69822 EAW75724 | ||||||||||||||||||