Human (GRCh38.p14)
Description

solute carrier family 5 member 2 [Source:HGNC Symbol;Acc:HGNC:11037]

Gene Synonyms

SGLT2

Location

Chromosome 16: 31,483,002-31,490,860 forward strand.

GRCh38:CM000678.2

About this gene

This gene has 9 transcripts (splice variants), 197 orthologues, 11 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000330498.4SLC5A2-2012267672aaENSP00000327943.3
 
Protein coding
CCDS10714P31639-1 NM_003041.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000569576.5SLC5A2-209516148aaENSP00000455143.1
 
Protein coding
H3BP44 -TSL:4CDS 3' incomplete
ENST00000419665.6SLC5A2-2021852458aaENSP00000410601.2
 
Nonsense mediated decay
P31639-2 -TSL:1
ENST00000564197.1SLC5A2-204498No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000567051.1SLC5A2-206334No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000568188.1SLC5A2-2072467No protein-
 
Retained intron
--TSL:2
ENST00000562006.1SLC5A2-203995No protein-
 
Retained intron
--TSL:3
ENST00000568891.1SLC5A2-208660No protein-
 
Retained intron
--TSL:5
ENST00000565446.1SLC5A2-205449No protein-
 
Retained intron
--TSL:5