We need your help! Has Ensembl saved you time or effort? Please take 15 minutes to fill in a survey and help EMBL-EBI make the case for why open data resources are critical to life science research.
https://www.surveymonkey.com/r/QGFMBH8?channel=[webpage]

Human (GRCh38.p14)
Description

solute carrier family 22 member 12 [Source:HGNC Symbol;Acc:HGNC:17989]

Gene Synonyms

HURAT1, OAT4L, RST, UAT, URAT1

Location

Chromosome 11: 64,590,641-64,602,353 forward strand.

GRCh38:CM000673.2

About this gene

This gene has 5 transcripts (splice variants), 468 orthologues, 22 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000377574.6SLC22A12-2042792553aaENSP00000366797.1
 
Protein coding
CCDS8075Q96S37-1 NM_144585.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000377572.5SLC22A12-2032887445aaENSP00000366795.1
 
Protein coding
CCDS60836Q96S37-2 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000377567.6SLC22A12-2022599445aaENSP00000366790.2
 
Protein coding
CCDS60836Q96S37-2 -GENCODE PrimaryGENCODE BasicTSL:5
ENST00000473690.5SLC22A12-2052522332aaENSP00000438437.1
 
Protein coding
Q96S37-3 -GENCODE PrimaryGENCODE BasicTSL:2
ENST00000336464.7SLC22A12-2011854519aaENSP00000336836.7
 
Protein coding
CCDS60835Q96S37-4 -GENCODE PrimaryGENCODE BasicTSL:1