Human (GRCh38.p14) ▼
Description

solute carrier family 31 member 2 [Source:HGNC Symbol;Acc:HGNC:11017]

Gene Synonyms

COPT2, CTR2, HCTR2

Location

Chromosome 9: 113,150,951-113,164,140 forward strand.

GRCh38:CM000671.2

About this gene

This gene has 10 transcripts (splice variants), 220 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000259392.8SLC31A2-2011723143aaENSP00000259392.3
 
Protein coding
CCDS6788O15432 Q53X94 NM_001860.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00001139225.1SLC31A2-2101779143aaENSP00000802995.1
 
Protein coding
CCDS6788Q53X94 -Ensembl Canonical ExtendedGENCODE BasicAPPRIS P1
ENST00001094861.1SLC31A2-2061675153aaENSP00000764667.1
 
Protein coding
--GENCODE Basic
ENST00001094864.1SLC31A2-209158734aaENSP00000764670.1
 
Protein coding
--GENCODE Basic
ENST00001094862.1SLC31A2-207149792aaENSP00000764668.1
 
Protein coding
--GENCODE Basic
ENST00001094860.1SLC31A2-205119395aaENSP00000764666.1
 
Protein coding
--GENCODE Basic
ENST00001094863.1SLC31A2-208108972aaENSP00000764669.1
 
Protein coding
--GENCODE Basic
ENST00001003680.1SLC31A2-204220846aaENSP00000673497.1
 
Nonsense mediated decay
---
ENST00000374220.3SLC31A2-202175073aaENSP00000363337.3
 
Nonsense mediated decay
F2Z3D2 -TSL:3
ENST00000490809.1SLC31A2-203771No protein-
 
Protein coding CDS not defined
--TSL:2