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Human (GRCh38.p14)
Description

solute carrier family 17 member 9 [Source:HGNC Symbol;Acc:HGNC:16192]

Gene Synonyms

C20ORF59, FLJ23412, VNUT

Location

Chromosome 20: 62,952,707-62,969,585 forward strand.

GRCh38:CM000682.2

About this gene

This gene has 7 transcripts (splice variants), 257 orthologues, 12 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000370351.9SLC17A9-2023518436aaENSP00000359376.4
 
Protein coding
CCDS42901Q9BYT1-1 NM_022082.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000370349.7SLC17A9-2012594430aaENSP00000359374.3
 
Protein coding
CCDS77600Q9BYT1-2 -GENCODE BasicTSL:1
ENST00000411611.1SLC17A9-203565152aaENSP00000388215.1
 
Protein coding
Q5W197 -TSL:2CDS 3' incomplete
ENST00000488738.5SLC17A9-2073992No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000459704.6SLC17A9-2042015No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000483113.1SLC17A9-2051624No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000487303.1SLC17A9-206507No protein-
 
Protein coding CDS not defined
--TSL:2