1. Gene
  2. NPR3 - natriuretic peptide receptor 3 Gene

NPR3 - natriuretic peptide receptor 3 Gene

中文名称:利钠肽受体 3

种属: Homo sapiens

同用名: NPRC; ANP-C; ANPRC; BOMOS; NPR-C; ANPR-C; GUCY2B; C5orf23

基因 ID: 4883 | 基因类型: protein coding

关于 NPR3

Cytogenetic location: 5p13.3 Genomic coordinates (GRCh38): 5:32,690,872-32,791,720 (from NCBI)

This gene has 7 transcripts (splice variants), 211 orthologues, 17 paralogues and is associated with 2 phenotypes. Biased expression in kidney (RPKM 35.4), fat (RPKM 14.2) and 8 other tissues.

功能概要

该基因编码三种利尿钠肽受体之一。利钠肽是调节血容量和压力、肺动脉高压和心脏功能以及一些代谢和生长过程的小肽。该基因的产物编码利钠肽受体,负责通过受体的内吞作用清除循环和细胞外利钠肽。已发现该基因编码不同异构体的多个转录变体。[RefSeq 提供,2011 年 2 月]

This gene encodes one of three natriuretic peptide receptors. Natriutetic Peptides are small Peptides which regulate blood volume and pressure, pulmonary hypertension, and cardiac function as well as some metabolic and growth processes. The product of this gene encodes a natriuretic peptide receptor responsible for clearing circulating and extracellular natriuretic Peptides through endocytosis of the receptor. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2011]

NPR3 基因产物(6)

mRNA Protein Name
NM_000908.4 NP_000899.1 atrial natriuretic peptide receptor 3 isoform 2 precursor
NM_001204375.2 NP_001191304.1 atrial natriuretic peptide receptor 3 isoform 1 precursor
NM_001204376.2 NP_001191305.1 atrial natriuretic peptide receptor 3 isoform 3
NM_001363652.2 NP_001350581.1 atrial natriuretic peptide receptor 3 isoform 4
NM_001364458.2 NP_001351387.1 atrial natriuretic peptide receptor 3 isoform 5
NM_001364460.2 NP_001351389.1 atrial natriuretic peptide receptor 3 isoform 6
基因本体论
  • 分子功能
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables chloride ion binding IDA
IDA: 通过直接分析推断
16870210 GOA
enables hormone binding IPI
IPI: 通过物理相互作用推断
16870210 GOA
enables natriuretic peptide receptor activity IDA
IDA: 通过直接分析推断
1660465 GOA
enables peptide binding IPI
IPI: 通过物理相互作用推断
16870210 GOA
enables peptide hormone binding IPI
IPI: 通过物理相互作用推断
1660465 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
16870210 GOA
enables protein homodimerization activity IDA
IDA: 通过直接分析推断
16870210 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of protein-containing complex IDA
IDA: 通过直接分析推断
16870210 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

NPR3 蛋白结构

ANF_receptor

ANF_receptor: Receptor family ligand binding region (71 - 422)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 541 a.a.
蛋白主名 其他名称

atrial natriuretic peptide receptor 3

atrial natriuretic peptide clearance receptor

重组 NPR3 蛋白

目录号 产品名 蛋白编号 纯度
HY-P71122 NPR3 Protein, Human (HEK293, Fc) P17342-1 (T24-E481) ≥95%

NPR3 抗体

目录号 产品名 应用 反应物种
HY-P81796 NPR3 Antibody (YA1541) WB, FC Human, Mouse, Rat

关联疾病

疾病名称 别名
Boudin-Mortier Syndrome

BOMOS

Tall Stature And Long Digits With Extra Epiphyses

Ischemic Colitis

Colitis, Ischemic

Irreversible Ischaemic Colitis

Anismus
Acromesomelic Dysplasia

Acromesomelic Dwarfism

Dysplasia, Acromesomelic

Acromesomelic Dysplasia Hunter-Thompson Type

Functional Diarrhea

Functional Diarrhoea

Acromesomelic Dysplasia 1

Acromesomelic Dysplasia, Maroteaux Type

Amdm

Acromesomelic Dysplasia 1, Maroteaux Type

AMD1

St. Helena Dysplasia

Acromesomelic Dysplasia-1

Acromesomelic Dysplasia Maroteaux Type

Acromesomelic Dwarfism Maroteux Type

Dysplasia, Acromesomelic, Type 1, Maroteaux

Acromesomelic Dysplasia Hunter-Thompson Type

Hypertension, Essential

Essential Hypertension

Hypertension

High Blood Pressure

Hypertension, Essential, Susceptibility To

Hypertensive Disease

Primary Hypertension

EHT

Hypertension, Salt-Sensitive Essential, Susceptibility To

Hyperpiesia

Idiopathic Hypertension

Hypertensive Disorder

Hypertension, Essential, Susceptibility To, 3

Hypertension, Essential 3

Hypertension, Essential, Salt-Sensitive

Hypertension, Essential, Susceptibility To, 6

Hypertension, Essential 6

Hypertension, Salt-Sensitive Essential

Hypertension, Susceptibility To

Hypertension, Essential, Susceptibility To, 4

Hypertension, Essential 4

Hypertension, Essential, Susceptibility To, 2

Hypertension, Essential 2

Hypertension, Essential, Susceptibility To, 1

Hypertension, Essential 1

Hypertension, Essential, Susceptibility To, 5

Hypertension, Essential 5

Htn

Vascular Hypertensive Disorder

Systemic Primary Arterial Hypertension

Hbp - [High Blood Pressure]

Systemic Arterial Hypertensive Disorder

Elevated Blood Pressure

Arterial Hypertension Nos

Hypertension Nos

Benign Hypertension

Systemic Arterial Hypertension

Systemic Hypertension

Artery Htn

Benign Htn

Vascular Htn

Vascular Hypertension

Cholesterol Hypertension

Cholesterol Htn

Idiopathic Htn

Malignant Hypertension

Malignant Htn

Raised Blood Pressure

Cardiovascular Hypertension

Primary Htn - [Hypertension]

High Arterial Tension

High Blood Pressure Disorder

Ht - [Hypertension]

Htn - [Hypertension]

Hypertensive Vascular Disease

Hypertensive Vascular Degeneration

Pulmonary Hypertension

Primary Pulmonary Hypertension

Hypertension Pulmonary

Hypertension, Pulmonary

Hypertension, Pulmonary, Primary

Idiopathic Pulmonary Hypertension

Idiopathic Pulmonary Arterial Hypertension

Pulmonary Htn - [Hypertension]

Secretory Diarrhea
Pheochromocytoma

Pheochromocytoma, Susceptibility To

Phaeochromocytoma

Adrenal Gland Chromaffin Paraganglioma

Adrenal Gland Chromaffinoma

Adrenal Gland Paraganglioma

Adrenal Gland Pheochromocytoma

Chromaffin Paraganglioma Of The Adrenal Gland

Intraadrenal Paraganglioma

PCC

Chromaffin Cell Tumor

Medullary Chromaffinoma

Medullary Paraganglioma

Pheochromoblastoma

Pheochromocytomas

Chromaffin Cell Neoplasm

Pheochromocytoma, Malignant

Volvulus Of Midgut

Volvulus

Intestinal Volvulus

Intestinal Malrotation, Familial

Familial Intestinal Malrotation

Twist Of Intestine, Bowel, Or Colon

Constipation
Heart Disease

Heart Failure

Congenital Heart Disease

Heart Diseases

Congenital Heart Defects

Congenital Heart Defect

Heart Malformation

Congenital Anomaly Of Heart

Heart Defect

Heart-Congenital Defect

Congenital Heart Disorder

Heart Defects Congenital

Heart Defects, Congenital

Heart Defects

Heart Disease, Congenital

Disease, Heart, Congenital

Congestive Heart Failure

Body Mass Index Quantitative Trait Locus 11

OBESITY

Obesity, Susceptibility To

Leanness, Inherited

Obesity, Susceptibility To, Bmiq11

Obesity, Mild, Early-Onset

Obesity, Association With

Obesity, Early-Onset, Susceptibility To

Obesity, Severe

Obesity, Severe, And Type Ii Diabetes

Obesity, Late-Onset

Obesity , Susceptibility To

BMIQ11

Obesity Bmiq11

Obesity, Early-Onset

Simple Obesity Nos

Excess Fat

Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified

Adiposis

疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

直系同源

种属 基因名 来源 基因 ID
Mus musculus NPR3 MGD MGI:97373
Rattus norvegicus NPR3 RGD RGD:3196
Canis familiaris NPR3 VGNC VGNC:58320
Macaca mulatta NPR3 VGNC VGNC:75390
Felis catus NPR3 VGNC VGNC:68535
Others NPR3 NCBI