SLC2A10: Difference between revisions

SLC2A10
Identifiers
Aliases	SLC2A10, ATS, GLUT10, solute carrier family 2 member 10, ATORS
External IDs	OMIM: 606145 MGI: 2156687 HomoloGene: 38551 GeneCards: SLC2A10
Gene location (Human)
Chr.	Chromosome 20 (human)
End	46,736,347 bp
Gene location (Mouse)
Chr.	Chromosome 2 (mouse)
End	165,361,837 bp
RNA expression pattern
	Top expressed in
	tibia; ; bronchial epithelial cell; ; stromal cell of endometrium; ; palpebral conjunctiva; ; right lobe of liver; ; prostate; ; periodontal fiber; ; seminal vesicula; ; minor salivary glands; ; right lobe of thyroid gland;
	Top expressed in
	pyloric antrum; ; epithelium of stomach; ; ascending aorta; ; aortic valve; ; mucous cell of stomach; ; calvaria; ; secondary oocyte; ; body of femur; ; seminal vesicula; ; trachea;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	glucose transmembrane transporter activity; carbohydrate:proton symporter activity; transmembrane transporter activity; transporter activity; D-glucose transmembrane transporter activity;
Cellular component	perinuclear region of cytoplasm; integral component of membrane; plasma membrane; membrane; endomembrane system; cytoplasm; integral component of plasma membrane;
Biological process	carbohydrate transport; glucose import; transmembrane transport; hexose transmembrane transport; proton transmembrane transport; glucose transmembrane transport;
	Sources:Amigo / QuickGO
Orthologs
	81031
	170441
	ENSG00000197496
	ENSMUSG00000027661
	O95528
	Q8VHD6
	NM_030777
	NM_130451
	NP_110404
	NP_569718
	Wikidata
View/Edit Human	View/Edit Mouse

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Latest revision as of 11:30, 4 March 2023

Solute carrier family 2, facilitated glucose transporter member 10 is a protein that in humans is encoded by the SLC2A10 gene.^[5]^[6]

SLC2A10 is a member of the facilitative glucose transporter family, which plays a significant role in maintaining glucose homeostasis.[supplied by OMIM]^[6]

References[edit]

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000197496 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000027661 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ McVie-Wylie AJ, Lamson DR, Chen YT (Mar 2001). "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 (1): 113–7. doi:10.1006/geno.2000.6457. PMID 11247674.
^ ^a ^b "Entrez Gene: SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10".

Further reading[edit]

Dawson PA, Mychaleckyj JC, Fossey SC, et al. (2001). "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 (1–2): 186–99. doi:10.1006/mgme.2001.3212. PMID 11592815.
Deloukas P, Matthews LH, Ashurst J, et al. (2002). "The DNA sequence and comparative analysis of human chromosome 20". Nature. 414 (6866): 865–71. Bibcode:2001Natur.414..865D. doi:10.1038/414865a. PMID 11780052.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Richardson S, Neama G, Phillips T, et al. (2003). "Molecular characterization and partial cDNA cloning of facilitative glucose transporters expressed in human articular chondrocytes; stimulation of 2-deoxyglucose uptake by IGF-I and elevated MMP-2 secretion by glucose deprivation". Osteoarthr. Cartil. 11 (2): 92–101. doi:10.1053/joca.2002.0858. PMID 12554125.
Wood IS, Hunter L, Trayhurn P (2003). "Expression of Class III facilitative glucose transporter genes (GLUT-10 and GLUT-12) in mouse and human adipose tissues". Biochem. Biophys. Res. Commun. 308 (1): 43–9. doi:10.1016/S0006-291X(03)01322-6. PMID 12890477.
Andersen G, Rose CS, Hamid YH, et al. (2003). "Genetic variation of the GLUT10 glucose transporter (SLC2A10) and relationships to type 2 diabetes and intermediary traits". Diabetes. 52 (9): 2445–8. doi:10.2337/diabetes.52.9.2445. PMID 12941788.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Zaidi SH, Peltekova V, Meyer S, et al. (2005). "A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13". Clin. Genet. 67 (2): 183–8. doi:10.1111/j.1399-0004.2004.00391.x. PMID 15679832. S2CID 21973630.
Mohlke KL, Skol AD, Scott LJ, et al. (2005). "Evaluation of SLC2A10 (GLUT10) as a candidate gene for type 2 diabetes and related traits in Finns". Mol. Genet. Metab. 85 (4): 323–7. doi:10.1016/j.ymgme.2005.04.011. PMID 15936967.
Segade F, Allred DC, Bowden DW (2005). "Functional characterization of the promoter of the human glucose transporter 10 gene". Biochim. Biophys. Acta. 1730 (2): 147–58. doi:10.1016/j.bbaexp.2005.06.012. PMID 16051383.
Coucke PJ, Willaert A, Wessels MW, et al. (2006). "Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome" (PDF). Nat. Genet. 38 (4): 452–7. doi:10.1038/ng1764. hdl:11379/29243. PMID 16550171. S2CID 836017.
Lin WH, Chuang LM, Chen CH, et al. (2006). "Association study of genetic polymorphisms of SLC2A10 gene and type 2 diabetes in the Taiwanese population". Diabetologia. 49 (6): 1214–21. doi:10.1007/s00125-006-0218-3. PMID 16586067.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000197496 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000027661 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid11247674-5] McVie-Wylie AJ, Lamson DR, Chen YT (Mar 2001). "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 (1): 113–7. doi:10.1006/geno.2000.6457. PMID 11247674.

[entrez-6] "Entrez Gene: SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10".

[1]

[2]

[3]

[4]

[5]

[6]

@@ Line 1: / Line 1: @@
+{{Short description|Protein-coding gene in the species Homo sapiens}}
 {{Infobox_gene}}
-'''Solute carrier family 2, facilitated glucose transporter member 10''' is a [[protein]] that in humans is encoded by the ''SLC2A10'' [[gene]].<ref name="pmid11247674">{{cite journal | vauthors = McVie-Wylie AJ, Lamson DR, Chen YT | title = 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 | journal = Genomics | volume = 72 | issue = 1 | pages = 113–7 |date=Mar 2001 | pmid = 11247674 | pmc =  | doi = 10.1006/geno.2000.6457 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=81031| accessdate = }}</ref>
+'''Solute carrier family 2, facilitated glucose transporter member 10''' is a [[protein]] that in humans is encoded by the ''SLC2A10'' [[gene]].<ref name="pmid11247674">{{cite journal | vauthors = McVie-Wylie AJ, Lamson DR, Chen YT | title = 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 | journal = Genomics | volume = 72 | issue = 1 | pages = 113–7 |date=Mar 2001 | pmid = 11247674 | doi = 10.1006/geno.2000.6457 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=81031}}</ref>
 SLC2A10 is a member of the facilitative glucose transporter family, which plays a significant role in maintaining glucose homeostasis.[supplied by OMIM]<ref name="entrez" />
@@ Line 15: / Line 16: @@
 {{refbegin | 2}}
 *{{cite journal   |vauthors=Dawson PA, Mychaleckyj JC, Fossey SC, etal |title=Sequence and functional analysis of GLUT10: a glucose transporter in the Type 2 diabetes-linked region of chromosome 20q12-13.1 |journal=Mol. Genet. Metab. |volume=74 |issue= 1–2 |pages= 186–99 |year= 2001 |pmid= 11592815 |doi= 10.1006/mgme.2001.3212 }}
-*{{cite journal   |vauthors=Deloukas P, Matthews LH, Ashurst J, etal |title=The DNA sequence and comparative analysis of human chromosome 20 |journal=Nature |volume=414 |issue= 6866 |pages= 865–71 |year= 2002 |pmid= 11780052 |doi= 10.1038/414865a }}
+*{{cite journal   |vauthors=Deloukas P, Matthews LH, Ashurst J, etal |title=The DNA sequence and comparative analysis of human chromosome 20 |journal=Nature |volume=414 |issue= 6866 |pages= 865–71 |year= 2002 |pmid= 11780052 |doi= 10.1038/414865a |bibcode=2001Natur.414..865D |doi-access= free }}
-*{{cite journal   |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899  | pmc=139241 }}
+*{{cite journal   |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899  | pmc=139241 |bibcode=2002PNAS...9916899M |doi-access=free }}
-*{{cite journal   |vauthors=Richardson S, Neama G, Phillips T, etal |title=Molecular characterization and partial cDNA cloning of facilitative glucose transporters expressed in human articular chondrocytes; stimulation of 2-deoxyglucose uptake by IGF-I and elevated MMP-2 secretion by glucose deprivation |journal=Osteoarthr. Cartil. |volume=11 |issue= 2 |pages= 92–101 |year= 2003 |pmid= 12554125 |doi=10.1053/joca.2002.0858  }}
+*{{cite journal   |vauthors=Richardson S, Neama G, Phillips T, etal |title=Molecular characterization and partial cDNA cloning of facilitative glucose transporters expressed in human articular chondrocytes; stimulation of 2-deoxyglucose uptake by IGF-I and elevated MMP-2 secretion by glucose deprivation |journal=Osteoarthr. Cartil. |volume=11 |issue= 2 |pages= 92–101 |year= 2003 |pmid= 12554125 |doi=10.1053/joca.2002.0858  |doi-access=free }}
 *{{cite journal  | vauthors=Wood IS, Hunter L, Trayhurn P |title=Expression of Class III facilitative glucose transporter genes (GLUT-10 and GLUT-12) in mouse and human adipose tissues |journal=Biochem. Biophys. Res. Commun. |volume=308 |issue= 1 |pages= 43–9 |year= 2003 |pmid= 12890477 |doi=10.1016/S0006-291X(03)01322-6  }}
-*{{cite journal   |vauthors=Andersen G, Rose CS, Hamid YH, etal |title=Genetic variation of the GLUT10 glucose transporter (SLC2A10) and relationships to type 2 diabetes and intermediary traits |journal=Diabetes |volume=52 |issue= 9 |pages= 2445–8 |year= 2003 |pmid= 12941788 |doi=10.2337/diabetes.52.9.2445  }}
+*{{cite journal   |vauthors=Andersen G, Rose CS, Hamid YH, etal |title=Genetic variation of the GLUT10 glucose transporter (SLC2A10) and relationships to type 2 diabetes and intermediary traits |journal=Diabetes |volume=52 |issue= 9 |pages= 2445–8 |year= 2003 |pmid= 12941788 |doi=10.2337/diabetes.52.9.2445  |doi-access=free }}
-*{{cite journal   |vauthors=Ota T, Suzuki Y, Nishikawa T, etal |title=Complete sequencing and characterization of 21,243 full-length human cDNAs |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
+*{{cite journal   |vauthors=Ota T, Suzuki Y, Nishikawa T, etal |title=Complete sequencing and characterization of 21,243 full-length human cDNAs |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 |doi-access= free }}
 *{{cite journal   |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |title=The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC) |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504  | pmc=528928 }}
-*{{cite journal   |vauthors=Zaidi SH, Peltekova V, Meyer S, etal |title=A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13 |journal=Clin. Genet. |volume=67 |issue= 2 |pages= 183–8 |year= 2005 |pmid= 15679832 |doi= 10.1111/j.1399-0004.2004.00391.x }}
+*{{cite journal   |vauthors=Zaidi SH, Peltekova V, Meyer S, etal |title=A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13 |journal=Clin. Genet. |volume=67 |issue= 2 |pages= 183–8 |year= 2005 |pmid= 15679832 |doi= 10.1111/j.1399-0004.2004.00391.x |s2cid=21973630 }}
 *{{cite journal  | vauthors=Mohlke KL, Skol AD, Scott LJ  | author-link=Karen Mohlke  |title=Evaluation of SLC2A10 (GLUT10) as a candidate gene for type 2 diabetes and related traits in Finns |journal=Mol. Genet. Metab. |volume=85 |issue= 4 |pages= 323–7 |year= 2005 |pmid= 15936967 |doi= 10.1016/j.ymgme.2005.04.011 |display-authors=etal}}
 *{{cite journal  | vauthors=Segade F, Allred DC, Bowden DW |title=Functional characterization of the promoter of the human glucose transporter 10 gene |journal=Biochim. Biophys. Acta |volume=1730 |issue= 2 |pages= 147–58 |year= 2005 |pmid= 16051383 |doi= 10.1016/j.bbaexp.2005.06.012 }}
-*{{cite journal   |vauthors=Coucke PJ, Willaert A, Wessels MW, etal |title=Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome |journal=Nat. Genet. |volume=38 |issue= 4 |pages= 452–7 |year= 2006 |pmid= 16550171 |doi= 10.1038/ng1764 |hdl=11379/29243 }}
+*{{cite journal   |vauthors=Coucke PJ, Willaert A, Wessels MW, etal |title=Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome |journal=Nat. Genet. |volume=38 |issue= 4 |pages= 452–7 |year= 2006 |pmid= 16550171 |doi= 10.1038/ng1764 |hdl=11379/29243 |s2cid=836017 |url=https://iris.unibs.it/bitstream/11379/29243/1/NAT.GEN-06.pdf |hdl-access=free }}
-*{{cite journal   |vauthors=Lin WH, Chuang LM, Chen CH, etal |title=Association study of genetic polymorphisms of SLC2A10 gene and type 2 diabetes in the Taiwanese population |journal=Diabetologia |volume=49 |issue= 6 |pages= 1214–21 |year= 2006 |pmid= 16586067 |doi= 10.1007/s00125-006-0218-3 }}
+*{{cite journal   |vauthors=Lin WH, Chuang LM, Chen CH, etal |title=Association study of genetic polymorphisms of SLC2A10 gene and type 2 diabetes in the Taiwanese population |journal=Diabetologia |volume=49 |issue= 6 |pages= 1214–21 |year= 2006 |pmid= 16586067 |doi= 10.1007/s00125-006-0218-3 |doi-access= free }}
 {{refend}}

Latest revision as of 11:30, 4 March 2023

See also[edit]

References[edit]

Further reading[edit]