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Human (GRCh37.p13)
Description

solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1 [Source:HGNC Symbol;Acc:11075]

Gene Synonyms

EBP50, NHERF, NHERF-1, NHERF1, NPHLOP2

Location

Chromosome 17: 72,744,791-72,765,492 forward strand.

GRCh37:CM000679.1

About this gene

This gene has 5 transcripts (splice variants), 3 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000262613.5SLC9A3R1-0011969358aaENSP00000262613.5
 
Protein coding
CCDS11705B3KY21 O14745 NM_004252.4Ensembl CanonicalGENCODE basic
ENST00000413388.2SLC9A3R1-0021285202aaENSP00000464982.1
 
Protein coding
B3KY21 -GENCODE basic
ENST00000583369.1SLC9A3R1-006841215aaENSP00000464321.1
 
Protein coding
J3QRP6 -CDS 3' incomplete
ENST00000581356.1SLC9A3R1-00551935aaENSP00000464117.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000578958.1SLC9A3R1-004714No protein-
 
Retained intron
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