2. Gene
  3. RAB3B - RAB3B, member RAS oncogene family Gene

RAB3B - RAB3B, member RAS oncogene family Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens
Gene ID: 5865 | Gene type: protein coding

About RAB3B

Cytogenetic location: 1p32.3 Genomic coordinates (GRCh38): 1:51,907,956-51,990,700 (from NCBI)

This gene has 1 transcript (splice variant), 197 orthologues and 68 paralogues. Biased expression in prostate (RPKM 6.0), brain (RPKM 3.4) and 11 other tissues.

Summary

Enables GDP binding activity; GTPase activity; and Myosin V binding activity. Involved in several processes, including positive regulation of dopamine uptake involved in synaptic transmission; regulation of synaptic vesicle cycle; and regulation of vesicle size. Located in perinuclear region of cytoplasm and vesicle. Is active in dopaminergic synapse. Is anchored component of synaptic vesicle membrane. [provided by Alliance of Genome Resources, Apr 2022]

RAB3B Products(1)

mRNA Protein Name
NM_002867.4 NP_002858.2 ras-related protein Rab-3B
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables GDP binding IDA
IDA: Inferred from direct assay
22321395 GOA
enables GTPase activity IDA
IDA: Inferred from direct assay
24891604 GOA
enables myosin V binding IPI
IPI: Inferred from physical interaction
24006491 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
24891604 GOA
Biological Process GO Annotation Evidence Reference Source
involved in antigen processing and presentation IMP
IMP: Inferred from mutant phenotype
19717423 GOA
involved in positive regulation of dopamine uptake involved in synaptic transmission IDA
IDA: Inferred from direct assay
20007772 GOA
involved in regulation of synaptic vesicle cycle IDA
IDA: Inferred from direct assay
20007772 GOA
involved in regulation of synaptic vesicle cycle IMP
IMP: Inferred from mutant phenotype
20007772 GOA
involved in regulation of vesicle size IDA
IDA: Inferred from direct assay
20007772 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cytoplasm IDA
IDA: Inferred from direct assay
20807725 GOA
is active in dopaminergic synapse IDA
IDA: Inferred from direct assay
20007772 GOA
is active in dopaminergic synapse IMP
IMP: Inferred from mutant phenotype
20007772 GOA
located in perinuclear region of cytoplasm IDA
IDA: Inferred from direct assay
19717423 GOA
is active in synaptic vesicle membrane IDA
IDA: Inferred from direct assay
20007772 GOA
is active in synaptic vesicle membrane IMP
IMP: Inferred from mutant phenotype
20007772 GOA
located in vesicle IDA
IDA: Inferred from direct assay
19717423 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

RAB3B Protein Structure

Ras

Ras: Ras family (24 - 183)

  • 0
  • 100
  • 200
  • 219 a.a.
Protein Preferred Names Protein Names

ras-related protein Rab-3B

brain antigen RAB3B

RAB3B Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
RAB3B P20337 VRTN Homo sapiens Q9H8Y1
Validated Y2H
32296183
Intra
RAB3B P20337 VRTN Homo sapiens Q9H8Y1
Y2H Array
32296183
Intra
RAB3B P20337 VRTN Homo sapiens Q9H8Y1
Y2H Prey Pooling
32296183
Intra
RAB3B P20337 RABIF Homo sapiens P47224
Y2H Prey Pooling
32296183
Intra
RAB3B P20337 RABIF Homo sapiens P47224
Validated Y2H
32296183
Intra
RAB3B P20337 RABIF Homo sapiens P47224
Y2H Array
32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

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
Immunodeficiency 54

Natural Killer Cell Deficiency, Familial Isolated

Primary Immunodeficiency With Natural-Killer Cell Deficiency And Adrenal Insufficiency

IMD54

Nkcd

Natural Killer Cell And Glucocorticoid Deficiency With Dna Repair Defect

Nkgcd

Familial Isolated Natural Killer Cell Deficiency

Primary Immunodeficiency Due To Mcm4 Deficiency
Kleefstra Syndrome 1

9q Subtelomeric Deletion Syndrome

KLEFS1

Chromosome 9q34.3 Deletion Syndrome

9q- Syndrome

9q34 Deletion Syndrome

Kleefstra Syndrome Due To 9q34 Microdeletion

Kleefstra Syndrome

9q-Syndrome

9qstds

Kleefstra Syndrome Due To 9q Subtelomeric Deletion

Kleefstra Syndrome Due To Del(9)(Q34)

Kleefstra Syndrome Due To Monosomy 9q34

Chromosome 9q Subtelomeric Deletion Syndrome

Kleefstra Syndrome, Type 1
Spinal Muscular Atrophy, Type Ii

SMA2

Sma Ii

Muscular Atrophy, Spinal, Intermediate Type

Muscular Atrophy, Spinal, Infantile Chronic Form

Intermediate Spinal Muscular Atrophy

Spinal Muscular Atrophy Type Ii

Spinal Muscular Atrophy-2

Spinal Muscular Atrophy 2

Spinal Muscular Atrophy Type 2

Dubowitz Disease

Proximal Spinal Muscular Atrophy Type 2

Sma Type 2

Sma Type Ii

Sma-Ii

Spinal Muscular Atrophy Infantile Chronic Form

Spinal Muscular Atrophy Intermediate Type

Spinal Muscular Atrophies Of Childhood

Atrophy, Muscular, Spinal, Type Ii

Muscular Atrophy, Spinal, Type Ii
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-RS11556 RAB3B Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus RAB3B MGD MGI:1917158
Bos taurus RAB3B VGNC VGNC:33650
Rattus norvegicus RAB3B RGD RGD:620922
Canis familiaris RAB3B VGNC VGNC:45283
Felis catus RAB3B VGNC VGNC:80334
Macaca mulatta RAB3B VGNC VGNC:81540