2. Gene
  3. ADARB2 - adenosine deaminase RNA specific B2 (inactive) Gene

ADARB2 - adenosine deaminase RNA specific B2 (inactive) Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：腺苷脱氨酶 RNA 特异性 B2 (无活性)

种属: Homo sapiens

同用名: RED2; ADAR3

基因 ID: 105 | 基因类型: protein coding

关于 ADARB2

Cytogenetic location: 10p15.3 Genomic coordinates (GRCh38): 10:1,177,313-1,737,525 (from NCBI)

This gene has 7 transcripts (splice variants), 279 orthologues and 14 paralogues. Biased expression in brain (RPKM 4.7), salivary gland (RPKM 0.5) and 3 other tissues.

功能概要

该基因编码 RNA 编辑酶的双链 RNA 腺苷脱氨酶家族的成员，并可能在 RNA 编辑中发挥调节作用。[RefSeq 提供，2008 年 7 月]

This gene encodes a member of the double-stranded RNA Adenosine Deaminase family of RNA-editing Enzymes and may play a regulatory role in RNA editing. [provided by RefSeq, Jul 2008]

ADARB2 基因产物(1)

mRNA Protein Name
NM_018702.4 NP_061172.1 double-stranded RNA-specific editase B2

ADARB2 蛋白结构

dsrm

dsrm: Double-stranded RNA binding motif (126 - 187)

dsrm

dsrm: Double-stranded RNA binding motif (287 - 339)

A_deamin

A_deamin: Adenosine-deaminase (editase) domain (408 - 731)

  • 0
  • 200
  • 400
  • 600
  • 739 a.a.
蛋白主名 其他名称

double-stranded RNA-specific editase B2

RED2 homolog

关联疾病

疾病名称 别名
Childhood Astrocytic Tumor

Juvenile Astrocytoma

Pediatric Astrocytoma
Dyschromatosis Symmetrica Hereditaria

Dyschromatosis Symmetrica Hereditaria 1

Reticulate Acropigmentation Of Dohi

DSH

Dsh1

Symmetric Dyschromatosis Of The Extremities

Rad

Familial Reticulate Acropigmentation Of Dohi

Acropigmentation Of Dohi

Symmetrical Dyschromatosis Of Extremities
Aicardi-Goutieres Syndrome

Aicardi Goutieres Syndrome

Cree Encephalitis

Aicardi-Goutières Syndrome

Encephalopathy With Basal Ganglia Calcification

Ags

Encephalopathy With Intracranial Calcification And Chronic Lymphocytosis Of Cerebrospinal Fluid

Pseudotoxoplasmosis Syndrome

Encephalopathy, Familial Infantile, With Calcification Of Basal Ganglia And Chronic Cerebrospinal Fluid Lymphocytosis

Familial Infantile Encephalopathy With Intracranial Calcification And Chronic Cerebrospinal Fluid Lymphocytosis

Aicardi-Goutieres Syndrome 1
Spinocerebellar Ataxia 8

Spinocerebellar Ataxia Type 8

SCA8

Ataxia, Spinocerebellar, Type 8
Amyotrophic Lateral Sclerosis 1

Amyotrophic Lateral Sclerosis

ALS

Lou Gehrig Disease

Amyotrophic Lateral Sclerosis Type 1

Charcot Disease

ALS1

Amyotrophic Lateral Sclerosis, Susceptibility To

Fals

Lou Gehrig'S Disease

Mnd

Motor Neuron Disease

Familial Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis 1, Familial

Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

Motor Neuron Disease, Bulbar

Motor Neurone Disease

Amyotrophic Lateral Sclerosis With Dementia

Dementia With Amyotrophic Lateral Sclerosis

Motor Neuron Disease, Amyotrophic Lateral Sclerosis

Sclerosis, Lateral, Amyotrophic

Sclerosis, Lateral, Amyotrophic, Type 1

Amyotrophic Sclerosis

Als - [Amyotrophic Lateral Sclerosis]

Wasting Palsy

Amyotrophic Paralysis

Amyotrophy Lateral Sclerosis

Wasting Paralysis

Spinal Progressive Amyotrophy

Progressive Atrophic Paralysis
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS00319 ADARB2 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Mus musculus ADARB2 MGD MGI:2151118
Macaca mulatta ADARB2 VGNC VGNC:100290
Felis catus ADARB2 VGNC VGNC:83490
Rattus norvegicus ADARB2 RGD RGD:621519
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