RAB5A - RAB5A, member RAS oncogene family Gene

Also Known as RAB5

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5868

About RAB5A

Cytogenetic location: 3p24.3 Genomic coordinates (GRCh38): 3:19,947,097-19,985,175 (from NCBI)

This gene has 8 transcripts (splice variants), 266 orthologues and 68 paralogues. Ubiquitous expression in brain (RPKM 22.0), thyroid (RPKM 19.7) and 25 other tissues.

Summary

Enables GDP binding activity; GTP binding activity; and GTPase activity. Involved in several processes, including amyloid-beta clearance by transcytosis; early endosome to late endosome transport; and regulation of exocytosis. Located in several cellular components, including cytoplasmic side of early endosome membrane; nucleoplasm; and terminal bouton. [provided by Alliance of Genome Resources, Apr 2022]

RAB5A Products (2)

mRNA Protein Name
NM_001292048.2 NP_001278977.1 ras-related protein Rab-5A isoform 2
NM_004162.5 NP_004153.2 ras-related protein Rab-5A isoform 1
Molecular Function GO Annotation Evidence References Source
enables GDP binding IDA
IDA: Inferred from direct assay
15378032 GOA
enables GTP binding IDA
IDA: Inferred from direct assay
15378032 GOA
enables GTPase activity IDA
IDA: Inferred from direct assay
15378032 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
7957092 GOA
Biological Process GO Annotation Evidence References Source
involved in amyloid-beta clearance by transcytosis IGI
IGI: Inferred from genetic interaction
26005850 GOA
involved in canonical Wnt signaling pathway IDA
IDA: Inferred from direct assay
16890161 GOA
involved in early endosome to late endosome transport IMP
IMP: Inferred from mutant phenotype
17562788 GOA
involved in endocytosis IDA
IDA: Inferred from direct assay
15378032 GOA
involved in modulation by host of viral process IMP
IMP: Inferred from mutant phenotype
19376974 GOA
involved in positive regulation of exocytosis IMP
IMP: Inferred from mutant phenotype
19966785 GOA
involved in receptor internalization IMP
IMP: Inferred from mutant phenotype
16890161 GOA
involved in regulation of endosome size IMP
IMP: Inferred from mutant phenotype
17562788 GOA
involved in regulation of filopodium assembly IDA
IDA: Inferred from direct assay
14978216 GOA
involved in regulation of synaptic vesicle exocytosis IMP
IMP: Inferred from mutant phenotype
16141272 GOA
involved in synaptic vesicle recycling IDA
IDA: Inferred from direct assay
16141272 GOA
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
18034774 GOA
located in cytoplasmic side of early endosome membrane IMP
IMP: Inferred from mutant phenotype
23382462 GOA
located in cytosol IDA
IDA: Inferred from direct assay
23382462 GOA
located in early endosome IDA
IDA: Inferred from direct assay
15078902 GOA
located in endosome membrane IDA
IDA: Inferred from direct assay
15016378 GOA
located in somatodendritic compartment IDA
IDA: Inferred from direct assay
16141272 GOA
located in terminal bouton IDA
IDA: Inferred from direct assay
16141272 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

RAB5A Protein Structure

Ras

Ras: Ras family (22 - 181)

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

ras-related protein Rab-5A

  • RAS-associated protein RAB5A

RAB5A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
RAB5A P20339 PNMA5 Homo sapiens Q96PV4 32814053
Intra
RAB5A P20339 PNMA5 Homo sapiens Q96PV4 32814053
Intra
RAB5A P20339 PNMA5 Homo sapiens Q96PV4 32814053
Intra
RAB5A P20339 MBIP Homo sapiens Q9NS73-5 32814053
Intra
RAB5A P20339 MBIP Homo sapiens Q9NS73-5 32814053
Intra
RAB5A P20339 MBIP Homo sapiens Q9NS73-5 32814053
Intra
RAB5A P20339 ALS2 Homo sapiens Q96Q42 21300063
Intra
RAB5A P20339 SUN2 Homo sapiens Q9UH99 26496610
Intra
RAB5A P20339 SUN2 Homo sapiens Q9UH99 31980649
Intra
RAB5A P20339 SYNC Homo sapiens Q9H7C4 32814053
Intra
RAB5A P20339 SYNC Homo sapiens Q9H7C4 32814053
Intra
RAB5A P20339 SYNC Homo sapiens Q9H7C4 32814053
Intra
RAB5A P20339 TCF3 Homo sapiens P15923-3 32814053
Intra
RAB5A P20339 TCF3 Homo sapiens P15923-3 32814053
Intra
RAB5A P20339 TCF3 Homo sapiens P15923-3 32814053
Intra
RAB5A P20339 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
RAB5A P20339 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
RAB5A P20339 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
RAB5A P20339 ANKFY1 Homo sapiens Q9P2R3 15328530
Intra
RAB5A P20339 EEA1 Homo sapiens Q15075
Y2H
10491193
Intra
RAB5A P20339 EEA1 Homo sapiens Q15075
Y2H
9697774
Intra
RAB5A P20339 PPP1R21 Homo sapiens Q6ZMI0 37267906
Intra
RAB5A P20339 OCRL Homo sapiens Q01968
GMS
21378754
Intra
RAB5A P20339 OCRL Homo sapiens Q01968 16902405
Intra
RAB5A P20339 INCA1 Homo sapiens Q0VD86 32814053
Intra
RAB5A P20339 INCA1 Homo sapiens Q0VD86 32814053
Intra
RAB5A P20339 INCA1 Homo sapiens Q0VD86 32814053
Intra
RAB5A P20339 LAMTOR1 Homo sapiens Q6IAA8 32814053
Intra
RAB5A P20339 LAMTOR1 Homo sapiens Q6IAA8 32814053
Intra
RAB5A P20339 LAMTOR1 Homo sapiens Q6IAA8 32814053
Intra
RAB5A P20339 ZNF20 Homo sapiens P17024 32814053
Intra
RAB5A P20339 ZNF20 Homo sapiens P17024 32814053
Intra
RAB5A P20339 ZNF20 Homo sapiens P17024 32814053
Intra
RAB5A P20339 APPL1 Homo sapiens Q9UKG1
IF
17581628
Intra
RAB5A P20339 APPL1 Homo sapiens Q9UKG1 17581628
Intra
RAB5A P20339 APPL1 Homo sapiens Q9UKG1 32296183
Intra
RAB5A P20339 APPL1 Homo sapiens Q9UKG1 29568061
Intra
RAB5A P20339 CCDC120 Homo sapiens Q96HB5 32814053
Intra
RAB5A P20339 CCDC120 Homo sapiens Q96HB5 32814053
Intra
RAB5A P20339 CCDC120 Homo sapiens Q96HB5 32814053
Intra
RAB5A P20339 C1orf216 Homo sapiens Q8TAB5 32814053
Intra
RAB5A P20339 C1orf216 Homo sapiens Q8TAB5 32814053
Intra
RAB5A P20339 C1orf216 Homo sapiens Q8TAB5 32814053
Intra
RAB5A P20339 FANCG Homo sapiens O15287 32814053
Intra
RAB5A P20339 FANCG Homo sapiens O15287 32814053
Intra
RAB5A P20339 FANCG Homo sapiens O15287 32814053
Intra
RAB5A P20339 TCAP Homo sapiens O15273 32814053
Intra
RAB5A P20339 TCAP Homo sapiens O15273 32814053
Intra
RAB5A P20339 TCAP Homo sapiens O15273 32814053
Cross
RAB5A P20339 PIK3R1 Bos taurus P23727 15377662
Cross
RAB5A P20339 PIK3R1 Bos taurus P23727 15377662
Cross: Cross-species interaction Intra: Intraspecies interaction

RAB5A Antibodies

Cat. No. Product Name Application Reactivity
HY-P80293 Rab5a Antibody (YA112) WB, IHC-P Human, Mouse
HY-P84172 Rab5a Antibody (YA3869) WB, IHC-P, ICC/IF, FC, ELISA Human
HY-P84172A Rab5a Antibody (YA3869)(PBS only) WB, IHC-P, ICC/IF, FC, ELISA Human
HY-P86541 Rab5a Antibody (YA6233) WB, IHC-P, ICC/IF, IP, ELISA Human, Mouse, Rat

Related Diseases

Diseases Alias
Motor Neuron Disease
  • Anterior Horn Cell Disease

  • Motor Neuron Diseases

  • Mnd - [Motor Neurone Disease]

  • Lou Gehrig Disease

  • Creeping Palsy

  • Creeping Paralysis

  • Bulbar Motor Neuron Disease

  • Bulbar Syndrome

  • Anterior Horn Cell Disorder

  • Hereditary Motor Neuron Disease

Choroideremia
  • CHM

  • Tcd

  • Progressive Tapetochoroidal Dystrophy

  • Choroidal Sclerosis

  • Tapetochoroidal Dystrophy, Progressive

  • Progressive Choroidal Atrophy

  • Tapetochoroidal Dystrophy

Tuberous Sclerosis 2
  • Tsc2 Angiomyolipomas, Renal, Modifier Of

  • TSC2

  • Tuberous Sclerosis

  • Tuberous Sclerosis-2

  • Tuberous Sclerosis, Type 2

  • Ts

  • Tuberous Sclerosis Complex

Human Monocytic Ehrlichiosis
  • Ehrlichiosis Chafeensis

  • Hme

  • Human Ehrlichial Infection, Human Monocytic Type

Charcot-Marie-Tooth Disease, Axonal, Type 2b
  • Charcot-Marie-Tooth Disease Type 2b

  • CMT2B

  • Hmsn Iib

  • Hmsn2b

  • Charcot-Marie-Tooth Disease, Type 2b

  • Hereditary Motor And Sensory Neuropathy Iib

  • Autosomal Dominant Charcot-Marie-Tooth Disease Type 2b

  • Charcot-Marie-Tooth Neuropathy Type 2b

  • Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2b

  • Charcot-Marie-Tooth Neuropathy, Type 2b

  • Hereditary Motor And Sensory Nueropathy Iib

  • Cmt 2b

  • Charcot Marie Tooth Disease Type 2b

  • Charcot-Marie-Tooth Disease, Neuronal, Type 2b

  • Hereditary Motor And Sensory Neuropathy 2 B

  • Peripheral Sensory Neuropathy, Autosomal Dominant

  • Charcot-Marie-Tooth Disease 2b

  • Charcot-Marie-Tooth Disease Axonal Type 2b

  • Charcot-Marie-Tooth Disease Neuronal Type 2b

  • Peripheral Sensory Neuropathy Autosomal Dominant

  • Psn

Borna Disease
  • Enzootic Encephalomyelitis

Rabies
  • Lyssa

  • Hydrophobia

  • St Hubert Disease

Legionnaire Disease
  • Legionnaires' Disease

  • Legionnaires Disease

  • Legionnaire Disease, Susceptibility To

  • Legionella

  • Legionella Pneumonia

  • Infection By Legionella Pneumophilia

  • Legionnaire'S Disease

  • Legionellosis

  • Legionaire Disease, Susceptibility To

  • Legionnaires Pneumonia

Down Syndrome
  • Trisomy 21

  • Complete Trisomy 21 Syndrome

  • Down'S Syndrome

  • Trisomy 21 Syndrome

  • Down'S Syndrome - Trisomy 21

  • Downs Syndrome

  • G Trisomy

  • 47,Xx,+21

  • 47,Xy,+21

  • Trisomy G

  • Down Syndrome, Susceptibility To

  • Chromosome 21 Trisomy

  • Trisomy 21 Nos

  • Abnormal Autosomes 21

Lowe Oculocerebrorenal Syndrome
  • Lowe Syndrome

  • Oculocerebrorenal Syndrome

  • OCRL

  • Oculocerebrorenal Syndrome Of Lowe

  • Ocrl1

  • Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency

  • Lowe Disease

  • Phosphatidylinositol 4,5-Biphosphate 5-Phosphatase Deficiency

  • Cerebrooculorenal Syndrome

  • Phosphatidylinositol-4,5-Bisphosphate-5-Phosphatase Deficiency

  • Lowe Oculo-Cerebro-Renal Dystrophy

  • Lowe Oculo-Cerebro-Renal Syndrome

  • Lowe Oculocerebrorenal Dystrophy

  • Low

  • Chromosome 11p Deletion Syndrome

  • Oculocerebrorenal Dystrophy

  • Cerebro-Oculorenal Dystrophy

  • Ocrl1 - [Oculocerebrorenal Syndrome]

  • Lowe-Terrey-Maclachlan Syndrome

  • Renal-Oculocerebrodystrophy

Legionellosis
  • Legionella Infection

  • Pontiac Fever

  • Legionnaires' Disease

  • Infection By Legionella Pneumophilia

  • Legionella Pneumophila Infection

Diamond-Blackfan Anemia 20
  • DBA20

  • Rps15a-Related Diamond-Blackfan Anemia

Retinal Melanoma
  • Malignant Retinal Melanoma

  • Malignant Melanoma Of Retina

Human Granulocytic Anaplasmosis
  • Human Granulocytic Ehrlichiosis

  • Hge

  • Human Ehrlichial Infection, Human Granulocytic Type

  • Human Anaplasmosis Due To Anaplasma Phagocytophilum

Ehrlichiosis
  • Human Ehrlichiosis

  • He

  • Hey

Pontocerebellar Hypoplasia, Type 2e
  • Pontocerebellar Hypoplasia Type 2

  • Pontocerebellar Hypoplasia Type 2e

  • Pch2

  • PCH2E

  • Progressive Microcephaly From Birth Extrapyramidal Dyskinesia Chorea Epilepsy

  • Pontocerebellar Hypoplasia 2e

  • Pcca2

  • Progressive Cerebello-Cerebral Atrophy Type 2

  • Doid:0112328

  • Hypoplasia, Pontocerebellar, Type 2e

  • Pontocerebellar Hypoplasia, Type 2d

  • Pontocerebellar Hypoplasia Type 2a

Niemann-Pick Disease, Type C1
  • Niemann-Pick Disease, Type C

  • NPC1

  • Niemann-Pick Disease, Type D

  • Niemann-Pick Disease Type C1

  • Niemann-Pick Disease With Cholesterol Esterification Block

  • Niemann-Pick Disease, Subacute Juvenile Form

  • Neurovisceral Storage Disease With Vertical Supranuclear Ophthalmoplegia

  • Npc

  • Niemann-Pick Disease, Chronic Neuronopathic Form

  • Niemann-Pick Disease Without Sphingomyelinase Deficiency

  • Niemann-Pick Disease Type C

  • Niemann-Pick Disease Type D

  • Niemann-Pick C1 Disease

  • Niemann-Pick Disease C1

  • Niemann-Pick Disease Chronic Neuronopathic Form

  • Niemann-Pick Disease Nova Scotian Type

  • Niemann-Pick Disease Subacute Juvenile Form

  • Niemann-Pick Disease Type Ii

  • Niemann-Picks Disease Type C

Carpenter Syndrome 1
  • Carpenter Syndrome

  • Acrocephalopolysyndactyly Type Ii

  • Acps Ii

  • CRPT1

  • Acrocephalopolysyndactyly Type 2

  • Acrocephalosyndactyly, Type Ii

  • Acrocephalopolysyndactyly 2

  • Acps2

  • Acps 2

  • Type Ii Acrocephalosyndactyly

  • Carpenter Syndrome, Type 1

  • Apert-Crouzon Disease

Parkinson Disease, Late-Onset
  • Parkinson Disease

  • Parkinson'S Disease

  • PD

  • PARK

  • Parkinson Disease, Susceptibility To

  • Late Onset Parkinson'S Disease

  • Late Onset Parkinson Disease

  • Paralysis Agitans

  • Primary Parkinsonism

  • Idiopathic Parkinson Disease

  • Parkinson'S

  • Parkinson Disease, Late-Onset, Susceptibility To

  • Parkinson Disease, Age Of Onset, Modifier

  • Lewy Body Parkinson Disease

  • Idiopathic Parkinson'S Disease

  • Pd - [Parkinson Disease]

  • Parkinson Disease Nos

  • Parkinson, Nos

  • Primary Parkinson Disease

Niemann-Pick Disease
  • Sphingomyelin/Cholesterol Lipidosis

  • Niemann-Pick Diseases

  • Lipoid Histiocytosis

  • Sphingomyelin Lipidosis

  • Sphingomyelinase Deficiency Disease

  • Lipid Histiocytosis

  • Neuronal Cholesterol Lipidosis

  • Neuronal Lipidosis

  • Npd

  • Sphingomyelinase Deficiency

  • Niemann-Pick Disease, Type A

Cystic Fibrosis
  • Mucoviscidosis

  • CF

  • Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis

  • Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis

  • Cystic Fibrosis Lung Disease, Modifier Of

  • Cystic Fibrosis Of Pancreas

  • Fibrocystic Disease Of Pancreas

  • Cf - [Cystic Fibrosis]

  • Cystic Fibrosis Nos

  • Fibrocystic Disease

  • Fibrocystic Disease Of The Pancreas

  • Mucoviscidosis Of Pancreas

  • Nonproliferative Fibrocystic Disease

  • Pancreatic Cystic Fibrosis

Hermansky-Pudlak Syndrome
  • Hps

  • Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells

  • Hermanski-Pudlak Syndrome

  • Hermansky Pudlak Syndrome

  • Platelet Storage Pool Deficiency

Alzheimer Disease, Familial, 1
  • Alzheimer Disease

  • Alzheimer'S Disease

  • Presenile And Senile Dementia

  • AD1

  • Alzheimer Disease, Susceptibility To

  • Alzheimer Disease, Late-Onset, Susceptibility To

  • Alzheimer Disease 1, Familial

  • AD

  • Familial Alzheimer Disease

  • Alzheimer Disease, Late-Onset

  • Alzheimers Dementia

  • Alzheimer Dementia

  • Alzheimer Sclerosis

  • Alzheimer Syndrome

  • Alzheimer-Type Dementia

  • Dat

  • Primary Senile Degenerative Dementia

  • Sdat

  • Alzheimer Disease 1

  • Autosomal Dominant Alzheimer Disease

  • Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

  • Late Onset Alzheimer Disease

  • Alzheimers Disease

  • Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

  • Late-Onset Alzheimers Disease

  • Alzheimer'S Disease Pathway Kegg

  • Dementia Due To Alzheimer'S Disease

  • Alzheimer Disease Type 1

  • Alzheimers

Neuronal Ceroid Lipofuscinosis
  • Hereditary Ceroid Lipofuscinosis

  • Batten Disease

  • Ncl

  • Neuronal Ceroid-Lipofuscinoses

  • Lipofuscinosis, Ceroid, Neuronal

  • Juvenile Neuronal Ceroid Lipofuscinosis

  • Cerebromacular Dystrophy

  • Cerebromacular Degeneration

  • Ceroid-Lipofuscinosis

  • Ncl - [Neuronal Ceroid Lipofuscinosis]

  • Amaurotic Familial Idiocy

  • Amaurotic Idiocy

  • Amaurotic Idiot

  • Neuronal Lipofuscinosis

  • Pigmentary Retinal Lipoid Neuronal Heredodegeneration

Hereditary Spastic Paraplegia
  • Familial Spastic Paraplegia

  • Hereditary Spastic Paraparesis

  • Strumpell-Lorrain Disease

  • Familial Spastic Paraparesis

  • Hsp

  • Spg

  • Strümpell-Lorrain Disease

  • Spastic Paraplegia, Hereditary

  • French Settlement Disease

  • Strumpell-Lorrain Syndrome

  • Fsp

  • Spastic Paraplegia, Familial

  • Spastic Paraplegia Hereditary

  • Spastic Paraplegia 3, Autosomal Dominant

  • Spastic Paraparesis

  • Hereditary Spastic Paralysis

  • Familial Spastic Paralysis

  • Hereditary Spastic Ataxia

Charcot-Marie-Tooth Disease
  • Cmt

  • Hmsn

  • Hereditary Motor And Sensory Neuropathy

  • Pma

  • Cmt - Charcot-Marie-Tooth Disease

  • Charcot Marie Tooth Disease

  • Charcot-Marie-Tooth Hereditary Neuropathy

  • Charcot-Marie-Tooth Syndrome

  • Peroneal Muscular Atrophy

  • Hereditary Motor And Sensory Neuropathies

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

Nervous System Disease
  • Abnormality Of The Nervous System

  • Nervous System Diseases

  • Nervous System Disorder

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

Orthologs Information

Species Symbol Source ID
Rattus norvegicus RAB5A RGD RGD:620936
Bos taurus RAB5A VGNC VGNC:33658
Canis familiaris RAB5A VGNC VGNC:45291
Mus musculus RAB5A MGD MGI:105926
Others RAB5A NCBI