Human (GRCh37.p13)
Description

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

Gene Synonyms

HIMTP, LOC387601, MGC120420, UST6

Location
About this transcript

This transcript has 9 exons, is annotated with 10 domains and features, is associated with 29486 variant alleles and maps to 352 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000403374.2SLC22A25-2012327234aaENSP00000384208.2
 
Protein coding
H7BYX8 -GENCODE basic
ENST00000306494.6SLC22A25-0011692547aaENSP00000307443.6
 
Protein coding
CCDS31592Q6T423 NM_199352.3GENCODE basic
ENST00000528239.1SLC22A25-0023699202aaENSP00000431235.1
 
Nonsense mediated decay
A4IF28 -CDS 5' incomplete
ENST00000527057.1SLC22A25-0051788399aaENSP00000432242.1
 
Nonsense mediated decay
A4IF29 -CDS 5' incomplete
ENST00000525295.1SLC22A25-0041362156aaENSP00000435614.1
 
Nonsense mediated decay
E9PJ86 Q494Y1 --
Statistics

Exons: 9, Coding exons: 6, Transcript length: 2,327 bps, Translation length: 234 residues

Version

ENST00000403374.2

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.

GENCODE basic gene

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