Human (GRCh38.p14)
Description

solute carrier family 9 member B2 [Source:HGNC Symbol;Acc:HGNC:25143]

Gene Synonyms

FLJ23984, NHA2, NHEDC2

Location

Chromosome 4: 103,019,868-103,085,829 reverse strand.

GRCh38:CM000666.2

About this gene

This gene has 11 transcripts (splice variants), 293 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000394785.9SLC9B2-2026351537aaENSP00000378265.3
 
Protein coding
CCDS3662Q86UD5-1 NM_178833.7MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000362026.7SLC9B2-2012300537aaENSP00000354574.3
 
Protein coding
CCDS3662Q86UD5-1 -GENCODE basicAPPRIS P1TSL:1
ENST00000503103.5SLC9B2-2031911417aaENSP00000425385.1
 
Protein coding
CCDS75173B7Z676 -GENCODE basicTSL:2
ENST00000503230.5SLC9B2-2041826480aaENSP00000422477.1
 
Protein coding
CCDS75174E9PE63 -GENCODE basicTSL:2
ENST00000506288.5SLC9B2-2071115354aaENSP00000421943.1
 
Protein coding
A0A0C4DGB3 -TSL:1CDS 5' incomplete
ENST00000503818.1SLC9B2-205648143aaENSP00000426305.1
 
Protein coding
D6RGJ7 -TSL:4CDS 3' incomplete
ENST00000508136.1SLC9B2-208578112aaENSP00000423496.1
 
Nonsense mediated decay
D6R9P2 -TSL:3
ENST00000505838.1SLC9B2-206824No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000515424.5SLC9B2-211793No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000510976.1SLC9B2-209599No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000512806.1SLC9B2-210547No protein-
 
Protein coding CDS not defined
--TSL:4