Human (GRCh38.p14)
Description

solute carrier family 26 member 8 [Source:HGNC Symbol;Acc:HGNC:14468]

Gene Synonyms

TAT1

Location

Chromosome 6: 35,943,516-36,024,868 reverse strand.

GRCh38:CM000668.2

About this gene

This gene has 8 transcripts (splice variants), 110 orthologues, 9 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000490799.6SLC26A8-2083437970aaENSP00000417638.1
 
Protein coding
CCDS4813Q96RN1-1 NM_052961.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000355574.6SLC26A8-2013463970aaENSP00000347778.2
 
Protein coding
CCDS4813Q96RN1-1 -GENCODE basicAPPRIS P1TSL:2
ENST00000394602.6SLC26A8-2023144865aaENSP00000378100.2
 
Protein coding
CCDS4814Q96RN1-2 -GENCODE basicTSL:1
ENST00000480663.1SLC26A8-206582190aaENSP00000420488.1
 
Protein coding
C9JMV8 -TSL:4CDS 3' incomplete
ENST00000465492.1SLC26A8-2032104320aaENSP00000418107.1
 
Nonsense mediated decay
H7C4T4 -TSL:2CDS 5' incomplete
ENST00000469847.5SLC26A8-205740184aaENSP00000419700.1
 
Nonsense mediated decay
H7C5E6 -TSL:5CDS 5' incomplete
ENST00000486155.1SLC26A8-2072989No protein-
 
Retained intron
--TSL:2
ENST00000466805.5SLC26A8-2042876No protein-
 
Retained intron
--TSL:2