Human (GRCh37.p13)
Description

solute carrier family 26 (anion exchanger), member 9 [Source:HGNC Symbol;Acc:14469]

Location

Chromosome 1: 205,882,176-205,912,588 reverse strand.

GRCh37:CM000663.1

About this gene

This gene has 6 transcripts (splice variants), 10 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000367135.3SLC26A9-0014799791aaENSP00000356103.3
 
Protein coding
CCDS30990Q7LBE3 NM_052934.3GENCODE basic
ENST00000367134.2SLC26A9-2014616887aaENSP00000356102.2
 
Protein coding
CCDS30989B1AVM8 NM_134325.2GENCODE basic
ENST00000340781.4SLC26A9-0034510887aaENSP00000341682.4
 
Protein coding
CCDS30989B1AVM8 -GENCODE basic
ENST00000491127.1SLC26A9-0024063No protein-
 
Retained intron
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ENST00000469392.1SLC26A9-005899No protein-
 
Retained intron
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ENST00000461505.1SLC26A9-006571No protein-
 
Retained intron
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