Human (GRCh38.p14)
Description

solute carrier family 22 member 25 [Source:HGNC Symbol;Acc:HGNC:32935]

Gene Synonyms

HIMTP, MGC120420, UST6

Location

Chromosome 11: 63,158,437-63,243,599 reverse strand.

GRCh38:CM000673.2

About this gene

This gene has 4 transcripts (splice variants), 845 orthologues and 22 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000306494.11SLC22A25-2018192547aaENSP00000307443.6
 
Protein coding
CCDS31592Q6T423 NM_199352.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000528239.5SLC22A25-2043699202aaENSP00000431235.1
 
Nonsense mediated decay
H0YCA2 -TSL:1CDS 5' incomplete
ENST00000527057.5SLC22A25-2031788399aaENSP00000432242.1
 
Nonsense mediated decay
H0YCS4 -TSL:1CDS 5' incomplete
ENST00000525295.1SLC22A25-2021362156aaENSP00000435614.1
 
Nonsense mediated decay
E9PJ86 -TSL:1