Human (GRCh38.p14)
Description

solute carrier family 7 member 11 [Source:HGNC Symbol;Acc:HGNC:11059]

Gene Synonyms

XCT

Location

Chromosome 4: 138,164,097-138,242,349 reverse strand.

GRCh38:CM000666.2

About this gene

This gene has 2 transcripts (splice variants), 287 orthologues and 12 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000280612.9SLC7A11-2019645501aaENSP00000280612.5
 
Protein coding
CCDS3742Q9UPY5 NM_014331.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000509248.1SLC7A11-20279775aaENSP00000424046.1
 
Nonsense mediated decay
H0Y9F9 -TSL:5CDS 5' incomplete