SLC9A3R1

GENERAL INFORMATION

? »

Gene name

SLC9A3R1

Gene description

Solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1

Protein class

Disease related genes
Plasma proteins
Potential drug targets
Predicted intracellular proteins
Transporters

Predicted localization

Intracellular

Number of transcripts

3
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic and membranous expression in glandular cells.

ANTIBODY RELIABILITY

? »

Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 3 antibodies.
HPA009672 , HPA027247 , CAB001962
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis

Endometrium



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

? »

Gene name

SLC9A3R1 (HGNC Symbol)

Synonyms

EBP50, NHERF

Description

Solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1 (HGNC Symbol)

Entrez gene summary

This gene encodes a sodium/hydrogen exchanger regulatory cofactor. The protein interacts with and regulates various proteins including the cystic fibrosis transmembrane conductance regulator and G-protein coupled receptors such as the beta2-adrenergic receptor and the parathyroid hormone 1 receptor. The protein also interacts with proteins that function as linkers between integral membrane and cytoskeletal proteins. The protein localizes to actin-rich structures including membrane ruffles, microvilli, and filopodia. Mutations in this gene result in hypophosphatemic nephrolithiasis/osteoporosis type 2, and loss of heterozygosity of this gene is implicated in breast cancer.[provided by RefSeq, Sep 2009]

Chromosome

17

Cytoband

q25.1

Chromosome location (bp)

74748652 - 74769353

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000109062 (version 78.38)

Entrez gene

9368

UniProt

O14745 (UniProt - Evidence at protein level)

neXtProt

NX_O14745

Antibodypedia

SLC9A3R1 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000262613
 
ENST00000413388
 
ENST00000583369
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

SLC9A3R1-001 ENSP00000262613
ENST00000262613
O14745
Show all »
Show » Show » 358 38.9 No 0
SLC9A3R1-002 ENSP00000464982
ENST00000413388
O14745
Show all »
Show » Show » 202 22 No 0
SLC9A3R1-006 ENSP00000464321
ENST00000583369
J3QRP6
Show all »
Show » Show » 215 22.9 No 0