RAB3D - RAB3D, member RAS oncogene family Gene

Homo sapiens

Also known as GOV; D2-2; RAB16; RAD3D

Gene ID: 9545 | Gene type: protein coding

About 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.

Summary

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 Products(1)

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

RAB3D Protein Structure

Ras

0
100
200
219 a.a.

Protein Preferred Names

Protein Names

ras-related protein Rab-3D

Rab3D upregulated with myeloid differentiation

Related Diseases

Diseases

Alias

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

Diseases	Alias
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

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS11558	RAB3D Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	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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