Human (GRCh38.p14)
Description

solute carrier family 9 member A9 [Source:HGNC Symbol;Acc:HGNC:20653]

Gene Synonyms

FLJ35613, NHE9

Location

Chromosome 3: 143,265,222-143,848,485 reverse strand.

GRCh38:CM000665.2

About this gene

This gene has 5 transcripts (splice variants), 175 orthologues, 10 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000316549.11SLC9A9-2013564645aaENSP00000320246.6
 
Protein coding
CCDS33872Q8IVB4 NM_173653.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000474151.1SLC9A9-202579147aaENSP00000418627.1
 
Protein coding
C9IZP1 -TSL:4CDS 3' incomplete
ENST00000474727.2SLC9A9-20359161aaENSP00000419090.2
 
Nonsense mediated decay
F8WF83 -TSL:4
ENST00000498717.2SLC9A9-205712No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000483124.1SLC9A9-204569No protein-
 
Protein coding CDS not defined
--TSL:4