Human (GRCh38.p14)
Description

solute carrier family 22 member 7 [Source:HGNC Symbol;Acc:HGNC:10971]

Gene Synonyms

NLT, OAT2

Location

Chromosome 6: 43,295,694-43,305,538 forward strand.

GRCh38:CM000668.2

About this gene

This gene has 9 transcripts (splice variants), 409 orthologues and 22 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000372585.10SLC22A7-2022559548aaENSP00000361666.5
 
Protein coding
CCDS4893Q9Y694-1 NM_153320.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS ALT1TSL:5
ENST00000372589.7SLC22A7-2032549546aaENSP00000361670.3
 
Protein coding
CCDS4892Q9Y694-2 -GENCODE basicAPPRIS P4TSL:2
ENST00000372574.7SLC22A7-2011822539aaENSP00000361655.3
 
Protein coding
Q9Y694-3 -GENCODE basicTSL:1
ENST00000449231.5SLC22A7-205933278aaENSP00000411818.1
 
Protein coding
Q5T051 -TSL:5CDS 3' incomplete
ENST00000451757.5SLC22A7-206846147aaENSP00000416052.1
 
Protein coding
Q5T047 -TSL:3CDS 3' incomplete
ENST00000436107.1SLC22A7-204658211aaENSP00000393836.1
 
Protein coding
X6RDF7 -TSL:5CDS 3' incomplete
ENST00000487175.5SLC22A7-208847No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000498232.1SLC22A7-2091339No protein-
 
Retained intron
--TSL:1
ENST00000480882.5SLC22A7-207696No protein-
 
Retained intron
--TSL:3