Human (GRCh37.p13)
Description

solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9 [Source:HGNC Symbol;Acc:11067]

Gene Synonyms

BAT1, CSNU3

Location

Chromosome 19: 33,321,415-33,360,672 reverse strand.

GRCh37:CM000681.1

About this gene

This gene has 6 transcripts (splice variants), 7 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000023064.4SLC7A9-0011761487aaENSP00000023064.3
 
Protein coding
CCDS12425K7EIF5 P82251 NM_014270.4GENCODE basic
ENST00000590341.1SLC7A9-0061752487aaENSP00000464822.1
 
Protein coding
CCDS12425K7EIF5 P82251 -GENCODE basic
ENST00000587772.1SLC7A9-0021568487aaENSP00000468439.1
 
Protein coding
CCDS12425K7EIF5 P82251 -GENCODE basic
ENST00000590465.1SLC7A9-003199839aaENSP00000468076.1
 
Nonsense mediated decay
K7EKD0 --
ENST00000592232.1SLC7A9-004103039aaENSP00000465563.1
 
Nonsense mediated decay
K7EKD0 --
ENST00000589659.1SLC7A9-005886No protein-
 
Retained intron
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