Human (GRCh37.p13)
Description

solute carrier family 31 (copper transporter), member 2 [Source:HGNC Symbol;Acc:11017]

Gene Synonyms

COPT2, CTR2, hCTR2

Location

Chromosome 9: 115,913,222-115,926,417 forward strand.

GRCh37:CM000671.1

About this gene

This gene has 3 transcripts (splice variants) and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000259392.3SLC31A2-0011785143aaENSP00000259392.3
 
Protein coding
CCDS6788O15432 Q53X94 NM_001860.2GENCODE basic
ENST00000374220.3SLC31A2-003175073aaENSP00000363337.3
 
Nonsense mediated decay
F2Z3D2 --
ENST00000490809.1SLC31A2-002771No protein-
 
Processed transcript
---