Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Details on Person The human gene SLC5A2 encodes a sodium-dependent glucose tra...

Class:IdSummation:429582
_displayNameThe human gene SLC5A2 encodes a sodium-dependent glucose tra...
_timestamp2015-08-04 13:01:15
created[InstanceEdit:429634] Jassal, Bijay, 2009-07-17
modified[InstanceEdit:5336462] Jassal, Bijay, 2014-03-03
[InstanceEdit:5362135] Jassal, Bijay, 2014-04-14
[InstanceEdit:5658180] Jassal, Bijay, 2014-12-18
[InstanceEdit:5669285] D'Eustachio, Peter, 2015-01-30
[InstanceEdit:5673780] Jassal, Bijay, 2015-02-10
[InstanceEdit:6789777] Jassal, Bijay, 2015-08-04
textThe human gene SLC5A2 encodes a sodium-dependent glucose transporter, SGLT2 (Wells et al. 1992). SLC5A2 is expressed in many tissues but primarily in the kidney, specifically the renal proximal tubules (S1 and S2 segments). It is a low affinity, high capacity transporter of glucose across the apical membrane, with co-transport of Na+ ions in a 1:1 ratio. Unlike SGLT1, it doesn't transport galactose. SLC5A2 is the main transporter of glucose in the kidney, responsible for approximately 98% of glucose reabsorption (remainder by SGLT1). Defects in SLC5A2 are the cause of renal glucosuria (GLYS1), an autosomal recessive renal tubular disorder (Calado et al. 2004). A separate sodium dependent glucose transporter NAGLT1, was identified in the multifacilitator superfamily (MFS) and could be a transporter of glucose in kidney proximal tubules. Its rat orthologue, Naglt1, has been shown to mediate tubular reabsorption of glucose (Horiba et al. 2003). By similarity, SLC5A1, 4 and 9 are predicted proteins that transport glucose in a Na+-dependent manner.
(summation)[Reaction:429613] SLC5As, NAGLT1 cotransport Glc and Na+ from extracellular region to cytosol [Homo sapiens]
[Change default viewing format]
No pathways have been reviewed or authored by The human gene SLC5A2 encodes a sodium-dependent glucose tra... (429582)