Human (GRCh38.p14)
Description

solute carrier family 26 member 9 [Source:HGNC Symbol;Acc:HGNC:14469]

Location

Chromosome 1: 205,913,048-205,943,460 reverse strand.

GRCh38:CM000663.2

About this gene

This gene has 6 transcripts (splice variants), 181 orthologues, 9 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000367135.8SLC26A9-2034791791aaENSP00000356103.3
 
Protein coding
CCDS30990Q7LBE3-1 NM_052934.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000367134.2SLC26A9-2024616887aaENSP00000356102.2
 
Protein coding
CCDS30989Q7LBE3-2 -GENCODE basicTSL:5
ENST00000340781.8SLC26A9-2014510887aaENSP00000341682.4
 
Protein coding
CCDS30989Q7LBE3-2 -GENCODE basicTSL:1
ENST00000491127.5SLC26A9-2064063No protein-
 
Retained intron
--TSL:2
ENST00000469392.1SLC26A9-205899No protein-
 
Retained intron
--TSL:5
ENST00000461505.1SLC26A9-204571No protein-
 
Retained intron
--TSL:5