2. Gene
  3. RAB3D - RAB3D, member RAS oncogene family Gene

RAB3D - RAB3D, member RAS oncogene family Gene

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

中文名称：RAB3D，成员 RAS 致癌基因家族

种属: Homo sapiens

同用名: GOV; D2-2; RAB16; RAD3D

基因 ID: 9545 | 基因类型: protein coding

关于 RAB3D

Cytogenetic location: 19p13.2 Genomic coordinates (GRCh38): 19:11,322,068-11,339,657 (from NCBI)

This gene has 2 transcripts (splice variants), 259 orthologues and 68 paralogues. Ubiquitous expression in skin (RPKM 24.5), esophagus (RPKM 14.0) and 22 other tissues.

功能概要

启用肌球蛋白 V 结合活动。参与骨吸收和调节分泌途径的正调节。位于细胞质微管和分泌小泡中。 [由基因组资源联盟提供，2022 年 4 月]

Enables Myosin V binding activity. Involved in bone resorption and positive regulation of regulated secretory pathway. Located in cytoplasmic microtubule and secretory vesicle. [provided by Alliance of Genome Resources, Apr 2022]

RAB3D 基因产物(1)

mRNA Protein Name
NM_004283.4 NP_004274.1 ras-related protein Rab-3D

RAB3D 蛋白结构

Ras

Ras: Ras family (24 - 183)

  • 0
  • 100
  • 200
  • 219 a.a.
蛋白主名 其他名称

ras-related protein Rab-3D

Rab3D upregulated with myeloid differentiation

RAB3D 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
RAB3D O95716 RAB3IP Homo sapiens Q96QF0-7
Y2H Prey Pooling
32296183
种属内
RAB3D O95716 RAB3IP Homo sapiens Q96QF0-7
Y2H Array
32296183
种属内
RAB3D O95716 RAB3IP Homo sapiens Q96QF0-7
Validated Y2H
32296183
种属内
RAB3D O95716 VRTN Homo sapiens Q9H8Y1
Validated Y2H
32296183
种属内
RAB3D O95716 VRTN Homo sapiens Q9H8Y1
Y2H Array
32296183
种属内
RAB3D O95716 VRTN Homo sapiens Q9H8Y1
Y2H Prey Pooling
32296183
种属内
RAB3D O95716 RABIF Homo sapiens P47224
Validated Y2H
32296183
种属内
RAB3D O95716 SYTL4 Homo sapiens Q96C24
Y2H Prey Pooling
32296183
种属内
RAB3D O95716 SYTL4 Homo sapiens Q96C24
Validated Y2H
32296183
种属内
RAB3D O95716 SYTL4 Homo sapiens Q96C24
Y2H Array
32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Warburg Micro Syndrome 1

Warburg Micro Syndrome

Micro Syndrome

Warbm

WARBM1

Warburg Sjo Fledelius Syndrome

Warburg-Sjo-Fledelius Syndrome

Micro Syndrome 1

Microcephaly, Microcornea, Congenital Cataract, Intellectual Disability, Optic Atrophy And Hypogenitalism
Dacryoadenitis

Dacryocystitis
Glioblastoma

Glioblastoma Multiforme

Gbm

Adult Glioblastoma Multiforme

Grade Iv Adult Astrocytic Tumor

Primary Glioblastoma Multiforme

Spongioblastoma Multiforme

Adult Glioblastoma

Primary Glioblastoma
Short-Rib Thoracic Dysplasia 2 With Or Without Polydactyly

Asphyxiating Thoracic Dystrophy 2

SRTD2

Atd2

Jatd

Jeune Asphyxiating Thoracic Dystrophy

Jeune Syndrome 2
Leukoencephalopathy, Cystic, Without Megalencephaly

Cystic Leukoencephalopathy Without Megalencephaly

Rnaset2-Deficient Cystic Leukoencephalopathy

Rnase T2-Deficient Leukoencephalopathy

Clwm

Leukoencephalopathy With Bilateral Anterior Temporal Lobe Cysts

Infantile-Onset Rnaset2 Deficient Cystic Leukoencephalopathy

Lbatc

LCWM
Warburg Micro Syndrome 3

WARBM3

Micro Syndrome 3
Warburg Micro Syndrome 2

WARBM2

Micro Syndrome 2
Martsolf Syndrome 1

Martsolf Syndrome

Cataract-Intellectual Disability-Hypogonadism Syndrome

MARTS1

Marts

Cataract-Mental Retardation-Hypogonadism

Martsolf
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-RS11558 RAB3D Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Macaca mulatta RAB3D VGNC VGNC:81542
Felis catus RAB3D VGNC VGNC:102699
Canis familiaris RAB3D VGNC VGNC:45285
Mus musculus RAB3D MGD MGI:97844
Bos taurus RAB3D VGNC VGNC:33652
Rattus norvegicus RAB3D RGD RGD:620924
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