Human (GRCh38.p14)
Description

solute carrier family 26 member 7 [Source:HGNC Symbol;Acc:HGNC:14467]

Gene Synonyms

SUT2

Location

Chromosome 8: 91,209,494-91,398,155 forward strand.

GRCh38:CM000670.2

About this gene

This gene has 10 transcripts (splice variants), 135 orthologues and 9 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000276609.8SLC26A7-2015237656aaENSP00000276609.3
 
Protein coding
CCDS6254Q8TE54-1 NM_052832.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000617233.2SLC26A7-2105257656aaENSP00000482549.1
 
Protein coding
CCDS6254Q8TE54-1 -GENCODE basicAPPRIS P1TSL:5
ENST00000617078.3SLC26A7-2095094355aaENSP00000482686.1
 
Protein coding
CCDS75765A0A087WZI7 -GENCODE basicTSL:5
ENST00000523719.5SLC26A7-2082902656aaENSP00000428849.1
 
Protein coding
CCDS6254Q8TE54-1 -GENCODE basicAPPRIS P1TSL:2
ENST00000309536.6SLC26A7-2022656663aaENSP00000309504.2
 
Protein coding
CCDS6255Q8TE54-2 -GENCODE basicTSL:1
ENST00000522862.5SLC26A7-207818207aaENSP00000428881.1
 
Protein coding
E5RFH2 -TSL:5CDS 3' incomplete
ENST00000520818.5SLC26A7-205736237aaENSP00000428747.1
 
Protein coding
H0YB61 -TSL:3CDS 5' incomplete
ENST00000522181.5SLC26A7-2062638269aaENSP00000427712.1
 
Nonsense mediated decay
E5RGL8 -TSL:2
ENST00000520249.5SLC26A7-2044140No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000517930.1SLC26A7-203581No protein-
 
Protein coding CDS not defined
--TSL:4