RAB33A - RAB33A, member RAS oncogene family Gene

Homo sapiens

Also known as RabS10

Gene ID: 9363 | Gene type: protein coding

About RAB33A

Cytogenetic location: Xq26.1 Genomic coordinates (GRCh38): X:130,110,623-130,184,870 (from NCBI)

This gene has 1 transcript (splice variant), 183 orthologues and 68 paralogues. Biased expression in brain (RPKM 10.9), lymph node (RPKM 3.6) and 7 other tissues.

Summary

The protein encoded by this gene belongs to the small GTPase superfamily, Rab family. It is GTP-binding protein and may be involved in vesicle transport. [provided by RefSeq, Jul 2008]

RAB33A Products(1)

mRNA	Protein	Name
NM_004794.3	NP_004785.1	ras-related protein Rab-33A

RAB33A Protein Structure

Ras

0
100
200
237 a.a.

Protein Preferred Names

Protein Names

ras-related protein Rab-33A

Small GTP-binding protein S10

Related Diseases

Diseases

Alias

Combined Oxidative Phosphorylation Deficiency

Spondyloepimetaphyseal Dysplasia, X-Linked, With Hypomyelinating Leukodystrophy

SEMDHL	Leukoencephalopathy With Metaphyseal Chondrodysplasia
H-Smd	Leukoencephalopathy-Metaphyseal Chondrodysplasia Syndrome
Lkmcd	Semd, X-Linked, With Mental Deterioration
Leukoencephalopathy-Spondylometaphyseal Dysplasia Syndrome	Hypomyelination-Spondylometaphyseal Dysplasia Syndrome
X-Linked Spondyloepimetaphyseal Dysplasia With Hypomyelinating Leukodystrophy	Leukoencephalopathy-Spondyloepimetaphyseal Dysplasia Syndrome
Hypomyelination-Spondyloepimetaphyseal Dysplasia Syndrome	Leukoencephalopathy-Semd Syndrome
Semd X-Linked With Mental Deterioration

Deafness, X-Linked 5, With Peripheral Neuropathy

Deafness, X-Linked 5	DFNX5
Aunx1	Auditory Neuropathy, X-Linked, 1, With Peripheral Sensory Neuropathy
X-Linked Deafness 5	X-Linked Auditory Neuropathy With Peripheral Sensory Neuropathy Type 1
X-Linked Hsan With Deafness	X-Linked Auditory Neuropathy 1 With Peripheral Sensory Neuropathy
X-Linked Hereditary Sensory And Autonomic Neuropathy With Deafness	X-Linked Hsan With Hearing Loss
X-Linked Hereditary Sensory And Autonomic Neuropathy With Hearing Loss	Deafness, X-Linked, 5, With Peripheral Neuropathy
Deafness, X-Linked, Type 5

Combined Oxidative Phosphorylation Deficiency 6

Severe X-Linked Mitochondrial Encephalomyopathy	COXPD6
Mitochondrial Encephalomyopathy Due To Combined Oxidative Phosphorylation Defect 6	Mitochondrial Encephalomyopathy Due To Coxpd6
Encephalomyopathy, Mitochondrial, X-Linked	Encephalomyopathy Mitochondrial X-Linked
Oxidative Phosphorylation Deficiency, Combined, Type 6

Charcot-Marie-Tooth Disease X-Linked Recessive 4

Cmt4x	Cmtx4
Cowchock Syndrome	X-Linked Charcot-Marie-Tooth Disease Type 4
Axonal Motor Sensory Neuropathy With Deafness And Mental Retardation	Charcot-Marie-Tooth Disease With Deafness And Mental Retardation
Nadmr	Namsd

Charcot-Marie-Tooth Disease, X-Linked Recessive, 4, With Or Without Cerebellar Ataxia

Cowchock Syndrome	CMTX4
Cowck	Neuropathy, Axonal Motor-Sensory, With Deafness And Mental Retardation
Namsd	Nadmr
Charcot-Marie-Tooth Disease With Deafness And Mental Retardation	Charcot-Marie-Tooth Disease Deafness Mental Retardation
Charcot-Marie-Tooth Disease X-Linked Recessive 4

Hypomyelinating Leukodystrophy

Hld	Leukodystrophy, Hypomyelinating

Leukodystrophy

Leukodystrophies

Sensorineural Hearing Loss

Sensory Hearing Loss	Sensorineural Deafness
Sensorineural Hearing Loss Disorder	Hearing Loss, Sensorineural
Central Hearing Loss	High Frequency Deafness
High Frequency Hearing Loss	High-Frequency Hearing Loss
Perceptive Deafness	Perceptive Hearing Loss
Perceptive Hearing Loss Or Deafness	Hearing Loss Sensorineural
Deafness Sensorineural	Hearing Loss High-Frequency
Hearing Loss, Central	Hearing Loss, High-Frequency

Developmental And Epileptic Encephalopathy 33

DEE33	Epileptic Encephalopathy, Early Infantile, 33
Eiee33	Developmental And Epileptic Encephalopathy, 33
Early Infantile Epileptic Encephalopathy 33	Encephalopathy, Epileptic, Early Infantile, Type 33

Prostate Transitional Cell Carcinoma

Transitional Cell Carcinoma Of Prostate

Primary Prostate Urothelial Carcinoma

Dyggve-Melchior-Clausen Disease

Dyggve-Melchior-Clausen Syndrome	DMC
Dmc Disease	Pseudo-Morquio Disease Type I
Dmc Syndrome

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-RS11546	RAB33A Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	RAB33A	VGNC	VGNC:45275
Rattus norvegicus	RAB33A	RGD	RGD:1563280
Bos taurus	RAB33A	VGNC	VGNC:33642
Mus musculus	RAB33A	MGD	MGI:109493

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