1. Gene
  2. NOX3 - NADPH oxidase 3 Gene

NOX3 - NADPH oxidase 3 Gene

中文名称:NADPH 氧化酶 3

种属: Homo sapiens

同用名: MOX-2; GP91-3

基因 ID: 50508 | 基因类型: protein coding

关于 NOX3

Cytogenetic location: 6q25.3 Genomic coordinates (GRCh38): 6:155,395,368-155,455,839 (from NCBI)

This gene has 1 transcript (splice variant), 136 orthologues and 6 paralogues. Low expression observed in reference dataset.

功能概要

该基因编码 NADPH 氧化酶的 NOX 家族成员。这些酶具有产生超氧化物和其他活性氧 (ROS) 以及跨质膜传输电子的能力。家族成员产生的 ROS 涉及许多生物学功能,包括宿主防御、蛋白质翻译后加工、细胞信号传导、基因表达调节和细胞分化。该基因编码的蛋白质主要在内耳中表达,并参与耳石/耳石的生物发生,耳石是内耳的晶体结构,参与重力感知。[RefSeq 提供,2009 年 5 月]

This gene encodes a member of the NOX family of NADPH oxidases. These Enzymes have the capacity to generate superoxide and other Reactive Oxygen Species (ROS) and transport electrons across the plasma membrane. The ROS generated by family members have been implicated in numerous biological functions including host defense, posttranlational processing of proteins, cellular signaling, regulation of gene expression, and cell differentiation. The protein encoded by this gene is expressed predominantly in the inner ear and is involved in the biogenesis of otoconia/otolith, which are crystalline structures of the inner ear involved in the perception of gravity.[provided by RefSeq, May 2009]

NOX3 基因产物(1)

mRNA Protein Name
NM_015718.3 NP_056533.1 NADPH oxidase 3
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
15824103 GOA
enables superoxide-generating NAD(P)H oxidase activity IDA
IDA: 通过直接分析推断
15181005 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

NOX3 蛋白结构

Ferric_reduct

Ferric_reduct: Ferric reductase like transmembrane component (58 - 217)

FAD_binding_8

FAD_binding_8: FAD-binding domain (293 - 391)

NAD_binding_6

NAD_binding_6: Ferric reductase NAD binding domain (401 - 548)

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  • 568 a.a.
蛋白主名 其他名称

NADPH oxidase 3

NADPH oxidase catalytic subunit-like 3

关联疾病

疾病名称 别名
Drug-Induced Hearing Loss

Drug Induced Hearing Loss

Phagocyte Bactericidal Dysfunction

Phagocytic Dysfunction

Granulomatous Disease, Chronic, X-Linked

CGDX

Chronic Granulomatous Disease, X-Linked

X-Linked Chronic Granulomatous Disease

Cgd

Cytochrome B-Negative Granulomatous Disease, Chronic, X-Linked

Cdgx

X-Linked Chronic Cytochrome B-Negative Granulomatous Disease

Chronic Granulomatous Disease Cytochrome B-Negative X-Linked

Chronic Granulomatous Disease Cytochrome B-Positive X-Linked

Granulomatous Disease, Chronic, X-Linked, Variant

Chronic Granulomatous Disease

Cgd

Granulomatous Disease, Chronic

Autosomal Recessive Chronic Granulomatous Disease

X-Linked Chronic Granulomatous Disease

Bridges-Good Syndrome

Congenital Dysphagocytosis

Quie Syndrome

Chronic Septic Granulomatosis

Chronic Granulomatous Disorder

Granulomatous Disease Chronic

Granulomatous Disease, Chronic, X-Linked

Inflammatory Bowel Disease

Inflammatory Bowel Diseases

Bowel Disease, Inflammatory

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
Canis familiaris NOX3 VGNC VGNC:43904
Felis catus NOX3 VGNC VGNC:68523
Mus musculus NOX3 MGD MGI:2681162
Rattus norvegicus NOX3 RGD RGD:1303190
Macaca mulatta NOX3 VGNC VGNC:75375
Bos taurus NOX3 VGNC VGNC:32183