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Human (GRCh37.p13)
Description

solute carrier family 31 (copper transporter), member 1 [Source:HGNC Symbol;Acc:11016]

Gene Synonyms

COPT1, CTR1, hCTR1

Location

Chromosome 9: 115,983,808-116,028,674 forward strand.

GRCh37:CM000671.1

About this gene

This gene has 3 transcripts (splice variants), 1 paralogue and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000374212.4SLC31A1-0014744190aaENSP00000363329.4
 
Protein coding
CCDS6789O15431 Q9BT69 NM_001859.3Ensembl CanonicalGENCODE basic
ENST00000374210.6SLC31A1-201753188aaENSP00000363327.5
 
Protein coding
Q5T1M3 -GENCODE basic
ENST00000496650.1SLC31A1-003475No protein-
 
Processed transcript
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