Human (GRCh38.p14)
Description

solute carrier family 47 member 2 [Source:HGNC Symbol;Acc:HGNC:26439]

Gene Synonyms

FLJ31196, MATE2, MATE2-K

Location

Chromosome 17: 19,678,288-19,718,979 reverse strand.

GRCh38:CM000679.2

About this gene

This gene has 10 transcripts (splice variants), 280 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000433844.4SLC47A2-2032099566aaENSP00000391848.3
 
Protein coding
CCDS92273Q86VL8-3 NM_001099646.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000350657.9SLC47A2-2022285580aaENSP00000338084.6
 
Protein coding
CCDS58530Q86VL8-4 -GENCODE basicTSL:1
ENST00000325411.9SLC47A2-2012258602aaENSP00000326671.5
 
Protein coding
CCDS11211Q86VL8-1 -GENCODE basicTSL:1
ENST00000574239.5SLC47A2-2101962219aaENSP00000458694.1
 
Nonsense mediated decay
Q86VL8-6 -TSL:1
ENST00000463318.5SLC47A2-2052742No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000456947.3SLC47A2-2043114No protein-
 
Retained intron
--TSL:NA
ENST00000467379.1SLC47A2-2062538No protein-
 
Retained intron
--TSL:2
ENST00000467609.5SLC47A2-2072201No protein-
 
Retained intron
--TSL:2
ENST00000483510.2SLC47A2-208991No protein-
 
Retained intron
--TSL:2
ENST00000574220.5SLC47A2-209965No protein-
 
Retained intron
--TSL:1