Human (GRCh37.p13)
Description

solute carrier family 26 (anion exchanger), member 8 [Source:HGNC Symbol;Acc:14468]

Gene Synonyms

SPGF3, TAT1

Location

Chromosome 6: 35,911,291-35,992,645 reverse strand.

GRCh37:CM000668.1

About this gene

This gene has 8 transcripts (splice variants), 10 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000490799.1SLC26A8-0013653970aaENSP00000417638.1
 
Protein coding
CCDS4813Q96RN1 NM_052961.3GENCODE basic
ENST00000355574.2SLC26A8-0053463970aaENSP00000347778.2
 
Protein coding
CCDS4813Q96RN1 NM_001193476.1GENCODE basic
ENST00000394602.2SLC26A8-0063144865aaENSP00000378100.2
 
Protein coding
CCDS4814Q96RN1 NM_138718.2GENCODE basic
ENST00000480663.1SLC26A8-007582190aaENSP00000420488.1
 
Protein coding
C9JMV8 -CDS 3' incomplete
ENST00000465492.1SLC26A8-0022104320aaENSP00000418107.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000469847.1SLC26A8-008740184aaENSP00000419700.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000486155.1SLC26A8-0042989No protein-
 
Retained intron
---
ENST00000466805.1SLC26A8-0032876No protein-
 
Retained intron
---