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Solute carrier family 2, facilitated glucose transporter member 10 (Glucose transporter type 10) (GLUT-10)

 GTR10_HUMAN             Reviewed;         541 AA.
O95528; A8K4J6; Q3MIX5; Q9H4I6;
16-NOV-2001, integrated into UniProtKB/Swiss-Prot.
01-JUN-2001, sequence version 2.
12-SEP-2018, entry version 156.
RecName: Full=Solute carrier family 2, facilitated glucose transporter member 10;
AltName: Full=Glucose transporter type 10;
Short=GLUT-10;
Name=SLC2A10; Synonyms=GLUT10;
Homo sapiens (Human).
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
NCBI_TaxID=9606;
[1]
NUCLEOTIDE SEQUENCE [MRNA].
TISSUE=Liver;
PubMed=11247674; DOI=10.1006/geno.2000.6457;
McVie-Wylie A.J., Lamson D.R., Chen Y.T.;
"Molecular cloning of a novel member of the GLUT family of
transporters, SLC2A10 (GLUT10), localized on chromosome 20q13.1: a
candidate gene for NIDDM susceptibility.";
Genomics 72:113-117(2001).
[2]
NUCLEOTIDE SEQUENCE [MRNA], TISSUE SPECIFICITY, AND CHARACTERIZATION.
PubMed=11592815; DOI=10.1006/mgme.2001.3212;
Dawson P.A., Mychaleckyj J.C., Fossey S.C., Mihic S.J., Craddock A.L.,
Bowden D.W.;
"Sequence and functional analysis of GLUT10: a glucose transporter in
the Type 2 diabetes-linked region of chromosome 20q12-13.1.";
Mol. Genet. Metab. 74:186-199(2001).
[3]
NUCLEOTIDE SEQUENCE [MRNA].
Stavrides G.S., Hashim Y., Huckle E.J., Deloukas P.;
Submitted (JAN-2000) to the EMBL/GenBank/DDBJ databases.
[4]
NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
PubMed=14702039; DOI=10.1038/ng1285;
Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R.,
Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H.,
Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.,
Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K.,
Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A.,
Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M.,
Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y.,
Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M.,
Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K.,
Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S.,
Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J.,
Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.-O., Nomura Y.,
Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N.,
Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S.,
Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S.,
Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O.,
Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H.,
Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B.,
Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y.,
Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T.,
Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y.,
Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S.,
Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T.,
Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M.,
Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T.,
Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K.,
Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R.,
Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., Sugano S.;
"Complete sequencing and characterization of 21,243 full-length human
cDNAs.";
Nat. Genet. 36:40-45(2004).
[5]
NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
PubMed=11780052; DOI=10.1038/414865a;
Deloukas P., Matthews L.H., Ashurst J.L., Burton J., Gilbert J.G.R.,
Jones M., Stavrides G., Almeida J.P., Babbage A.K., Bagguley C.L.,
Bailey J., Barlow K.F., Bates K.N., Beard L.M., Beare D.M.,
Beasley O.P., Bird C.P., Blakey S.E., Bridgeman A.M., Brown A.J.,
Buck D., Burrill W.D., Butler A.P., Carder C., Carter N.P.,
Chapman J.C., Clamp M., Clark G., Clark L.N., Clark S.Y., Clee C.M.,
Clegg S., Cobley V.E., Collier R.E., Connor R.E., Corby N.R.,
Coulson A., Coville G.J., Deadman R., Dhami P.D., Dunn M.,
Ellington A.G., Frankland J.A., Fraser A., French L., Garner P.,
Grafham D.V., Griffiths C., Griffiths M.N.D., Gwilliam R., Hall R.E.,
Hammond S., Harley J.L., Heath P.D., Ho S., Holden J.L., Howden P.J.,
Huckle E., Hunt A.R., Hunt S.E., Jekosch K., Johnson C.M., Johnson D.,
Kay M.P., Kimberley A.M., King A., Knights A., Laird G.K., Lawlor S.,
Lehvaeslaiho M.H., Leversha M.A., Lloyd C., Lloyd D.M., Lovell J.D.,
Marsh V.L., Martin S.L., McConnachie L.J., McLay K., McMurray A.A.,
Milne S.A., Mistry D., Moore M.J.F., Mullikin J.C., Nickerson T.,
Oliver K., Parker A., Patel R., Pearce T.A.V., Peck A.I.,
Phillimore B.J.C.T., Prathalingam S.R., Plumb R.W., Ramsay H.,
Rice C.M., Ross M.T., Scott C.E., Sehra H.K., Shownkeen R., Sims S.,
Skuce C.D., Smith M.L., Soderlund C., Steward C.A., Sulston J.E.,
Swann R.M., Sycamore N., Taylor R., Tee L., Thomas D.W., Thorpe A.,
Tracey A., Tromans A.C., Vaudin M., Wall M., Wallis J.M.,
Whitehead S.L., Whittaker P., Willey D.L., Williams L., Williams S.A.,
Wilming L., Wray P.W., Hubbard T., Durbin R.M., Bentley D.R., Beck S.,
Rogers J.;
"The DNA sequence and comparative analysis of human chromosome 20.";
Nature 414:865-871(2001).
[6]
NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L.,
Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R.,
Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V.,
Hannenhalli S., Turner R., Yooseph S., Lu F., Nusskern D.R.,
Shue B.C., Zheng X.H., Zhong F., Delcher A.L., Huson D.H.,
Kravitz S.A., Mouchard L., Reinert K., Remington K.A., Clark A.G.,
Waterman M.S., Eichler E.E., Adams M.D., Hunkapiller M.W., Myers E.W.,
Venter J.C.;
Submitted (SEP-2005) to the EMBL/GenBank/DDBJ databases.
[7]
NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
TISSUE=Liver;
PubMed=15489334; DOI=10.1101/gr.2596504;
The MGC Project Team;
"The status, quality, and expansion of the NIH full-length cDNA
project: the Mammalian Gene Collection (MGC).";
Genome Res. 14:2121-2127(2004).
[8]
ASSOCIATION OF VARIANT THR-206 WITH LOWER SERUM INSULIN LEVEL.
PubMed=12941788; DOI=10.2337/diabetes.52.9.2445;
Andersen G., Rose C.S., Hamid Y.H., Drivsholm T., Borch-Johnsen K.,
Hansen T., Pedersen O.;
"Genetic variation of the GLUT10 glucose transporter (SLC2A10) and
relationships to type 2 diabetes and intermediary traits.";
Diabetes 52:2445-2448(2003).
[9]
VARIANT ATS ARG-81, AND SUBCELLULAR LOCATION.
PubMed=16550171; DOI=10.1038/ng1764;
Coucke P.J., Willaert A., Wessels M.W., Callewaert B., Zoppi N.,
De Backer J., Fox J.E., Mancini G.M.S., Kambouris M., Gardella R.,
Facchetti F., Willems P.J., Forsyth R., Dietz H.C., Barlati S.,
Colombi M., Loeys B., De Paepe A.;
"Mutations in the facilitative glucose transporter GLUT10 alter
angiogenesis and cause arterial tortuosity syndrome.";
Nat. Genet. 38:452-457(2006).
[10]
VARIANTS ATS TRP-132; VAL-142; GLN-231; GLU-246; TRP-426 AND LYS-437.
PubMed=17935213; DOI=10.1002/humu.20623;
Callewaert B.L., Willaert A., Kerstjens-Frederikse W.S., De Backer J.,
Devriendt K., Albrecht B., Ramos-Arroyo M.A., Doco-Fenzy M.,
Hennekam R.C.M., Pyeritz R.E., Krogmann O.N., Gillessen-kaesbach G.,
Wakeling E.L., Nik-zainal S., Francannet C., Mauran P., Booth C.,
Barrow M., Dekens R., Loeys B.L., Coucke P.J., De Paepe A.M.;
"Arterial tortuosity syndrome: clinical and molecular findings in 12
newly identified families.";
Hum. Mutat. 29:150-158(2008).
-!- FUNCTION: Facilitative glucose transporter.
-!- BIOPHYSICOCHEMICAL PROPERTIES:
Kinetic parameters:
KM=0.28 mM for 2-deoxy-D-glucose;
-!- SUBCELLULAR LOCATION: Endomembrane system
{ECO:0000269|PubMed:16550171}; Multi-pass membrane protein
{ECO:0000269|PubMed:16550171}. Cytoplasm, perinuclear region
{ECO:0000269|PubMed:16550171}.
-!- TISSUE SPECIFICITY: Widely expressed; highest levels in liver and
pancreas. {ECO:0000269|PubMed:11592815}.
-!- DISEASE: 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:0000269|PubMed:16550171,
ECO:0000269|PubMed:17935213}. Note=The disease is caused by
mutations affecting the gene represented in this entry.
-!- SIMILARITY: Belongs to the major facilitator superfamily. Sugar
transporter (TC 2.A.1.1) family. Glucose transporter subfamily.
{ECO:0000305}.
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EMBL; AF321240; AAK26294.1; -; mRNA.
EMBL; AF248053; AAK31911.1; -; mRNA.
EMBL; AL137188; CAB69822.2; -; mRNA.
EMBL; AK290961; BAF83650.1; -; mRNA.
EMBL; AL031055; -; NOT_ANNOTATED_CDS; Genomic_DNA.
EMBL; CH471077; EAW75724.1; -; Genomic_DNA.
EMBL; BC101657; AAI01658.1; -; mRNA.
EMBL; BC113423; AAI13424.1; -; mRNA.
CCDS; CCDS13402.1; -.
RefSeq; NP_110404.1; NM_030777.3.
UniGene; Hs.305971; -.
ProteinModelPortal; O95528; -.
BioGrid; 123350; 1.
STRING; 9606.ENSP00000352216; -.
DrugBank; DB09502; Fludeoxyglucose F-18.
TCDB; 2.A.1.1.59; the major facilitator superfamily (mfs).
iPTMnet; O95528; -.
PhosphoSitePlus; O95528; -.
BioMuta; SLC2A10; -.
EPD; O95528; -.
MaxQB; O95528; -.
PaxDb; O95528; -.
PeptideAtlas; O95528; -.
PRIDE; O95528; -.
ProteomicsDB; 50935; -.
DNASU; 81031; -.
Ensembl; ENST00000359271; ENSP00000352216; ENSG00000197496.
GeneID; 81031; -.
KEGG; hsa:81031; -.
UCSC; uc002xsl.4; human.
CTD; 81031; -.
DisGeNET; 81031; -.
EuPathDB; HostDB:ENSG00000197496.5; -.
GeneCards; SLC2A10; -.
HGNC; HGNC:13444; SLC2A10.
HPA; HPA041015; -.
MalaCards; SLC2A10; -.
MIM; 208050; phenotype.
MIM; 606145; gene.
neXtProt; NX_O95528; -.
OpenTargets; ENSG00000197496; -.
Orphanet; 3342; Arterial tortuosity syndrome.
PharmGKB; PA37769; -.
eggNOG; KOG0254; Eukaryota.
eggNOG; ENOG410XNQK; LUCA.
GeneTree; ENSGT00920000149002; -.
HOGENOM; HOG000202868; -.
HOVERGEN; HBG051858; -.
InParanoid; O95528; -.
KO; K08147; -.
OMA; GFLIDCY; -.
OrthoDB; EOG091G085H; -.
PhylomeDB; O95528; -.
TreeFam; TF332408; -.
Reactome; R-HSA-189200; Cellular hexose transport.
Reactome; R-HSA-5619068; Defective SLC2A10 causes arterial tortuosity syndrome (ATS).
ChiTaRS; SLC2A10; human.
GeneWiki; SLC2A10; -.
GenomeRNAi; 81031; -.
PRO; PR:O95528; -.
Proteomes; UP000005640; Chromosome 20.
Bgee; ENSG00000197496; Expressed in 179 organ(s), highest expression level in tibia.
CleanEx; HS_SLC2A10; -.
ExpressionAtlas; O95528; baseline and differential.
Genevisible; O95528; HS.
GO; GO:0012505; C:endomembrane system; IEA:UniProtKB-SubCell.
GO; GO:0016021; C:integral component of membrane; NAS:UniProtKB.
GO; GO:0048471; C:perinuclear region of cytoplasm; IEA:UniProtKB-SubCell.
GO; GO:0005886; C:plasma membrane; TAS:Reactome.
GO; GO:0005351; F:carbohydrate:proton symporter activity; IBA:GO_Central.
GO; GO:0055056; F:D-glucose transmembrane transporter activity; TAS:Reactome.
GO; GO:0005355; F:glucose transmembrane transporter activity; IBA:GO_Central.
GO; GO:0046323; P:glucose import; IBA:GO_Central.
GO; GO:1904659; P:glucose transmembrane transport; NAS:UniProtKB.
GO; GO:0008645; P:hexose transmembrane transport; TAS:Reactome.
CDD; cd06174; MFS; 1.
InterPro; IPR020846; MFS_dom.
InterPro; IPR005828; MFS_sugar_transport-like.
InterPro; IPR036259; MFS_trans_sf.
InterPro; IPR003663; Sugar/inositol_transpt.
InterPro; IPR005829; Sugar_transporter_CS.
Pfam; PF00083; Sugar_tr; 2.
PRINTS; PR00171; SUGRTRNSPORT.
SUPFAM; SSF103473; SSF103473; 2.
PROSITE; PS50850; MFS; 1.
PROSITE; PS00216; SUGAR_TRANSPORT_1; 2.
1: Evidence at protein level;
Complete proteome; Cytoplasm; Disease mutation; Glycoprotein;
Membrane; Polymorphism; Reference proteome; Sugar transport;
Transmembrane; Transmembrane helix; Transport.
CHAIN 1 541 Solute carrier family 2, facilitated
glucose transporter member 10.
/FTId=PRO_0000050379.
TOPO_DOM 1 15 Cytoplasmic. {ECO:0000255}.
TRANSMEM 16 36 Helical; Name=1. {ECO:0000255}.
TOPO_DOM 37 48 Extracellular. {ECO:0000255}.
TRANSMEM 49 69 Helical; Name=2. {ECO:0000255}.
TOPO_DOM 70 77 Cytoplasmic. {ECO:0000255}.
TRANSMEM 78 98 Helical; Name=3. {ECO:0000255}.
TOPO_DOM 99 106 Extracellular. {ECO:0000255}.
TRANSMEM 107 127 Helical; Name=4. {ECO:0000255}.
TOPO_DOM 128 134 Cytoplasmic. {ECO:0000255}.
TRANSMEM 135 155 Helical; Name=5. {ECO:0000255}.
TOPO_DOM 156 166 Extracellular. {ECO:0000255}.
TRANSMEM 167 187 Helical; Name=6. {ECO:0000255}.
TOPO_DOM 188 233 Cytoplasmic. {ECO:0000255}.
TRANSMEM 234 254 Helical; Name=7. {ECO:0000255}.
TOPO_DOM 255 269 Extracellular. {ECO:0000255}.
TRANSMEM 270 290 Helical; Name=8. {ECO:0000255}.
TOPO_DOM 291 298 Cytoplasmic. {ECO:0000255}.
TRANSMEM 299 319 Helical; Name=9. {ECO:0000255}.
TOPO_DOM 320 414 Extracellular. {ECO:0000255}.
TRANSMEM 415 435 Helical; Name=10. {ECO:0000255}.
TOPO_DOM 436 445 Cytoplasmic. {ECO:0000255}.
TRANSMEM 446 466 Helical; Name=11. {ECO:0000255}.
TOPO_DOM 467 476 Extracellular. {ECO:0000255}.
TRANSMEM 477 497 Helical; Name=12. {ECO:0000255}.
TOPO_DOM 498 541 Cytoplasmic. {ECO:0000255}.
CARBOHYD 334 334 N-linked (GlcNAc...) asparagine.
{ECO:0000255}.
VARIANT 81 81 S -> R (in ATS; dbSNP:rs80358230).
{ECO:0000269|PubMed:16550171}.
/FTId=VAR_029535.
VARIANT 106 106 A -> S (in dbSNP:rs6094438).
/FTId=VAR_029536.
VARIANT 132 132 R -> W (in ATS; dbSNP:rs121908173).
{ECO:0000269|PubMed:17935213}.
/FTId=VAR_042417.
VARIANT 142 142 G -> V (in ATS; dbSNP:rs864309480).
{ECO:0000269|PubMed:17935213}.
/FTId=VAR_042418.
VARIANT 206 206 A -> T (associated with lower insulin
level; dbSNP:rs2235491).
/FTId=VAR_029335.
VARIANT 225 225 R -> H (in dbSNP:rs34295241).
/FTId=VAR_042419.
VARIANT 231 231 R -> Q (in ATS; dbSNP:rs771028960).
{ECO:0000269|PubMed:17935213}.
/FTId=VAR_042420.
VARIANT 246 246 G -> E (in ATS; dbSNP:rs564317065).
{ECO:0000269|PubMed:17935213}.
/FTId=VAR_042421.
VARIANT 426 426 G -> W (in ATS; dbSNP:rs121908172).
{ECO:0000269|PubMed:17935213}.
/FTId=VAR_042422.
VARIANT 437 437 E -> K (in ATS; dbSNP:rs763220502).
{ECO:0000269|PubMed:17935213}.
/FTId=VAR_042423.
VARIANT 445 445 G -> E (in ATS; dbSNP:rs753723351).
/FTId=VAR_042424.
VARIANT 518 518 T -> A (in dbSNP:rs6018008).
/FTId=VAR_024652.
VARIANT 537 537 I -> V (in dbSNP:rs7348121).
/FTId=VAR_029537.
SEQUENCE 541 AA; 56911 MW; 6D644525FA136908 CRC64;
MGHSPPVLPL CASVSLLGGL TFGYELAVIS GALLPLQLDF GLSCLEQEFL VGSLLLGALL
ASLVGGFLID CYGRKQAILG SNLVLLAGSL TLGLAGSLAW LVLGRAVVGF AISLSSMACC
IYVSELVGPR QRGVLVSLYE AGITVGILLS YALNYALAGT PWGWRHMFGW ATAPAVLQSL
SLLFLPAGTD ETATHKDLIP LQGGEAPKLG PGRPRYSFLD LFRARDNMRG RTTVGLGLVL
FQQLTGQPNV LCYASTIFSS VGFHGGSSAV LASVGLGAVK VAATLTAMGL VDRAGRRALL
LAGCALMALS VSGIGLVSFA VPMDSGPSCL AVPNATGQTG LPGDSGLLQD SSLPPIPRTN
EDQREPILST AKKTKPHPRS GDPSAPPRLA LSSALPGPPL PARGHALLRW TALLCLMVFV
SAFSFGFGPV TWLVLSEIYP VEIRGRAFAF CNSFNWAANL FISLSFLDLI GTIGLSWTFL
LYGLTAVLGL GFIYLFVPET KGQSLAEIDQ QFQKRRFTLS FGHRQNSTGI PYSRIEISAA
S


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U2023m CLIA Glucose transporter type 4, insulin-responsive,Glut4,GLUT-4,Glut-4,GT2,Mouse,Mus musculus,Slc2a4,Solute carrier family 2, facilitated glucose transporter member 4 96T


 

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