NPR2

GENERAL INFORMATION

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Gene name

NPR2

Gene description

Natriuretic peptide receptor 2

Protein class

Disease related genes
Enzymes
FDA approved drug targets
Predicted intracellular proteins
Predicted membrane proteins

Predicted localization

Intracellular,Membrane

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Mixed
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Most normal tissues showed weak cytoplasmic staining or were negative. The adrenal gland showed strong cytoplasmic positivity. Hepatocytes, heart and skeletal muscle were moderately stained.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA011977
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RNA AND PROTEIN EXPRESSION SUMMARY

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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

Adrenal gland

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Mixed

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

NPR2 (HGNC Symbol)

Synonyms

AMDM, ANPb, ANPRB, GUCY2B, NPRB

Description

Natriuretic peptide receptor 2 (HGNC Symbol)

Entrez gene summary

This gene encodes natriuretic peptide receptor B, one of two integral membrane receptors for natriuretic peptides. Both NPR1 and NPR2 contain five functional domains: an extracellular ligand-binding domain, a single membrane-spanning region, and intracellularly a protein kinase homology domain, a helical hinge region involved in oligomerization, and a carboxyl-terminal guanylyl cyclase catalytic domain. The protein is the primary receptor for C-type natriuretic peptide (CNP), which upon ligand binding exhibits greatly increased guanylyl cyclase activity. Mutations in this gene are the cause of acromesomelic dysplasia Maroteaux type. [provided by RefSeq, Jul 2008]

Chromosome

9

Cytoband

p13.3

Chromosome location (bp)

35792154 - 35809732

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000159899 (version 78.38)

Entrez gene

4882

UniProt

P20594 (UniProt - Evidence at protein level)

neXtProt

NX_P20594

Antibodypedia

NPR2 antibodies


PROTEIN BROWSER

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ENST00000342694
 
ENST00000421267
 
ENST00000447210
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

NPR2-001 ENSP00000341083
ENST00000342694
P20594
Show all »
Show » Show » 1047 117 Yes 1
NPR2-003 ENSP00000399204
ENST00000421267
Show » Show » 275 30.9 No 0
NPR2-005 ENSP00000393029
ENST00000447210
H7C056
Show all »
Show » Show » 164 19 No 0