RAB33A - RAB33A, member RAS oncogene family Gene

中文名称：RAB33A，成员 RAS 致癌基因家族

种属: Homo sapiens

同用名: RabS10

基因 ID: 9363 | 基因类型: protein coding

关于 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.

功能概要

该基因编码的蛋白质属于小 GTPase 超家族 Rab 家族。它是 GTP 结合蛋白，可能参与囊泡运输。[RefSeq 提供，2008 年 7 月]

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 基因产物(1)

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

基因本体论

分子功能
生物过程

分子功能 GO 注释	逻辑证据	参考文献	来源
enables protein binding	IPI IPI: 通过物理相互作用推断	16189514	GOA

生物过程 GO 注释	逻辑证据	参考文献	来源
involved in antigen processing and presentation	IMP IMP: 通过突变表型推断	19717423	GOA

EXP：通过实验结果推断 IDA：通过直接分析推断 IPI：通过物理相互作用推断 IMP：通过突变表型推断 IGI：通过遗传相互作用推断 IEP：通过表达模式推断

RAB33A 蛋白结构

Ras

0
100
200
237 a.a.

蛋白主名

其他名称

ras-related protein Rab-33A

Small GTP-binding protein S10

RAB33A 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	RAB33A	Q14088	KRT34	Homo sapiens	O76011	Y2H Prey Pooling	32296183
种属内	RAB33A	Q14088	KRT34	Homo sapiens	O76011	Y2H Array	32296183
种属内	RAB33A	Q14088	LRP2BP	Homo sapiens	Q9P2M1	Y2H Array	32296183
种属内	RAB33A	Q14088	LRP2BP	Homo sapiens	Q9P2M1	Y2H Prey Pooling	32296183
种属内	RAB33A	Q14088	LRP2BP	Homo sapiens	Q9P2M1	Validated Y2H	32296183
种属内	RAB33A	Q14088	RUFY2	Homo sapiens	Q8WXA3-4	Validated Y2H	32296183
种属内	RAB33A	Q14088	RUFY2	Homo sapiens	Q8WXA3-4	Y2H Prey Pooling	32296183
种属内	RAB33A	Q14088	RUFY2	Homo sapiens	Q8WXA3-4	Y2H Array	32296183
种属内	RAB33A	Q14088	ATG16L1	Homo sapiens	Q676U5	Anti Tag CoIP	33961781
种属内	RAB33A	Q14088	ATG16L1	Homo sapiens	Q676U5	Y2H Prey Pooling	32296183
种属内	RAB33A	Q14088	ATG16L1	Homo sapiens	Q676U5	Validated Y2H	32296183
种属内	RAB33A	Q14088	ATG16L1	Homo sapiens	Q676U5	Y2H Array	32296183
种属内	RAB33A	Q14088	RABAC1	Homo sapiens	Q9UI14	Y2H Array	19060904
种属内	RAB33A	Q14088	RABAC1	Homo sapiens	Q9UI14	Y2H Pooling	19060904
种属内	RAB33A	Q14088	RABAC1	Homo sapiens	Q9UI14	Y2H Pooling	16189514
种属内	RAB33A	Q14088	ARL6IP1	Homo sapiens	Q15041	Y2H Prey Pooling	25416956
种属内	RAB33A	Q14088	RUFY3	Homo sapiens	Q7L099	Y2H Array	32296183
种属内	RAB33A	Q14088	RUFY3	Homo sapiens	Q7L099	Y2H Prey Pooling	32296183
种属内	RAB33A	Q14088	RUFY3	Homo sapiens	Q7L099	Validated Y2H	32296183
种属内	RAB33A	Q14088	LNX1	Homo sapiens	Q8TBB1	Validated Y2H	32296183
种属内	RAB33A	Q14088	LNX1	Homo sapiens	Q8TBB1	Y2H Prey Pooling	32296183
种属内	RAB33A	Q14088	LNX1	Homo sapiens	Q8TBB1	Y2H Array	32296183
种属内	RAB33A	Q14088	SIAH1	Homo sapiens	Q8IUQ4	Y2H Prey Pooling	25416956
种属内	RAB33A	Q14088	SIAH1	Homo sapiens	Q8IUQ4	Validated Y2H	25416956
种属内	RAB33A	Q14088	PSMF1	Homo sapiens	Q92530	Y2H Prey Pooling	32296183
种属内	RAB33A	Q14088	PSMF1	Homo sapiens	Q92530	Validated Y2H	32296183
种属内	RAB33A	Q14088	PSMF1	Homo sapiens	Q92530	Y2H Array	32296183
种属内	RAB33A	Q14088	KRT31	Homo sapiens	Q15323	Validated Y2H	32296183
种属内	RAB33A	Q14088	KRT31	Homo sapiens	Q15323	Y2H Prey Pooling	32296183
种属内	RAB33A	Q14088	KRT31	Homo sapiens	Q15323	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

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

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

Cat. No.	产品名	作用方式	纯度	是否罕见病
HY-RS11546	RAB33A Human Pre-designed siRNA Set A	Pre-designed Sets	/	否

直系同源

种属	基因名	来源	基因 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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站点地图隐私声明

沪ICP备15051369号-4

上海工商

沪公网安备31011502019417

沪(浦)应急管危经许[2021]201709(QFYS)

营业执照（三证合一）

RAB33A - RAB33A, member RAS oncogene family Gene

关于 RAB33A

功能概要

RAB33A 基因产物(1)

RAB33A 蛋白结构

RAB33A 蛋白互作信息

关联疾病

直系同源

热门区域

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RAB33A - RAB33A, member RAS oncogene family Gene

关于 RAB33A

功能概要

RAB33A 基因产物(1)

RAB33A 蛋白结构

RAB33A 蛋白互作信息

关联疾病

相关产品

直系同源

热门区域

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B

C

F

G

H

J

L

N

Q

S

T

X

Y

Z