Human (GRCh38.p14)
Description

solute carrier family 38 member 3 [Source:HGNC Symbol;Acc:HGNC:18044]

Gene Synonyms

G17, SN1, SNAT3

Location

Chromosome 3: 50,205,246-50,221,486 forward strand.

GRCh38:CM000665.2

About this gene

This gene has 9 transcripts (splice variants), 284 orthologues, 15 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000614032.5SLC38A3-2062953504aaENSP00000481301.1
 
Protein coding
CCDS74940Q99624 NM_006841.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000445096.5SLC38A3-204880216aaENSP00000480466.1
 
Protein coding
A0A087WWS5 -TSL:5CDS 3' incomplete
ENST00000621456.2SLC38A3-20863599aaENSP00000484379.1
 
Protein coding
A0A087X1Q4 -TSL:5CDS 3' incomplete
ENST00000610458.4SLC38A3-20558496aaENSP00000479737.1
 
Protein coding
A0A087WVW8 -TSL:3CDS 3' incomplete
ENST00000621714.4SLC38A3-209992104aaENSP00000483959.1
 
Nonsense mediated decay
A0A087X175 -TSL:5
ENST00000620404.1SLC38A3-207566No protein-
 
Retained intron
--TSL:3
ENST00000417121.2SLC38A3-201491No protein-
 
Retained intron
--TSL:5
ENST00000417851.2SLC38A3-202438No protein-
 
Retained intron
--TSL:3
ENST00000439524.2SLC38A3-203424No protein-
 
Retained intron
--TSL:3