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Human (GRCh38.p14)
Description

solute carrier family 6 member 3 [Source:HGNC Symbol;Acc:HGNC:11049]

Gene Synonyms

DAT, DAT1

Location

Chromosome 5: 1,392,794-1,445,514 reverse strand.

GRCh38:CM000667.2

View alleles of this gene on alternative sequences

About this gene

This gene has 8 transcripts (splice variants), 1 gene allele, 166 orthologues, 19 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000270349.12SLC6A3-2013942620aaENSP00000270349.9
 
Protein coding
CCDS3863Q01959 NM_001044.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000713696.1SLC6A3-2042595572aaENSP00000519000.1
 
Protein coding
A0AAQ5BGN6 -GENCODE PrimaryGENCODE Basic
ENST00000941790.1SLC6A3-2082554575aaENSP00000611849.1
 
Protein coding
--GENCODE Basic
ENST00000936841.1SLC6A3-2072386494aaENSP00000606900.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000713698.1SLC6A3-2061072247aaENSP00000519002.1
 
Protein coding
A0AAQ5BGS7 -GENCODE Basic
ENST00000713697.1SLC6A3-2052451379aaENSP00000519001.1
 
Nonsense mediated decay
A0AAQ5BGQ7 --
ENST00000512002.2SLC6A3-203950No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000511750.1SLC6A3-202556No protein-
 
Retained intron
--TSL:4