Human (GRCh38.p14)
Description

solute carrier family 7 member 9 [Source:HGNC Symbol;Acc:HGNC:11067]

Gene Synonyms

BAT1, CSNU3

Location

Chromosome 19: 32,830,509-32,869,767 reverse strand.

GRCh38:CM000681.2

About this gene

This gene has 6 transcripts (splice variants), 239 orthologues, 12 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000023064.9SLC7A9-2011766487aaENSP00000023064.3
 
Protein coding
CCDS12425P82251 NM_014270.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000590341.5SLC7A9-2041752487aaENSP00000464822.1
 
Protein coding
CCDS12425P82251 -GENCODE basicAPPRIS P1TSL:1
ENST00000587772.1SLC7A9-2021568487aaENSP00000468439.1
 
Protein coding
CCDS12425P82251 -GENCODE basicAPPRIS P1TSL:1
ENST00000590465.5SLC7A9-205199839aaENSP00000468076.1
 
Nonsense mediated decay
K7EKD0 -TSL:2
ENST00000592232.5SLC7A9-206103039aaENSP00000465563.1
 
Nonsense mediated decay
K7EKD0 -TSL:1
ENST00000589659.1SLC7A9-203886No protein-
 
Retained intron
--TSL:3