Human (GRCh38.p14)
Description

solute carrier family 22 member 6 [Source:HGNC Symbol;Acc:HGNC:10970]

Gene Synonyms

OAT1, PAHT, ROAT1

Location
About this transcript

This transcript has 10 exons, is annotated with 18 domains and features, is associated with 3922 variant alleles and maps to 465 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000360421.9SLC22A6-2012127550aaENSP00000353597.4
 
Protein coding
CCDS8041Q4U2R8-2 NM_153276.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000377871.7SLC22A6-2022151563aaENSP00000367102.3
 
Protein coding
CCDS31591Q4U2R8-1 -GENCODE basicTSL:1
ENST00000421062.2SLC22A6-2031560519aaENSP00000404441.2
 
Protein coding
CCDS44631Q4U2R8-4 -GENCODE basicTSL:1
ENST00000458333.6SLC22A6-2041521506aaENSP00000396401.2
 
Protein coding
CCDS44632Q4U2R8-3 -GENCODE basicTSL:1
ENST00000540654.5SLC22A6-2061778261aaENSP00000445946.1
 
Nonsense mediated decay
F5H0T7 -TSL:5
ENST00000537349.1SLC22A6-205768No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 10, Coding exons: 10, Transcript length: 1,560 bps, Translation length: 519 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q4U2R8

CCDS

This transcript is a member of the Human CCDS set: CCDS44631

Transcript Support Level (TSL)

TSL:1

Version

ENST00000421062.2

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.