CDC42 - cell division cycle 42 Gene

Also Known as TKS; G25K; CDC42Hs

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 998

About CDC42

Cytogenetic location: 1p36.12 Genomic coordinates (GRCh38): 1:22,052,709-22,101,360 (from NCBI)

This gene has 24 transcripts (splice variants), 237 orthologues, 22 paralogues and is associated with 4 phenotypes. Ubiquitous expression in bone marrow (RPKM 88.8), colon (RPKM 72.7) and 25 other tissues.

Summary

The protein encoded by this gene is a small GTPase of the Rho-subfamily, which regulates signaling pathways that control diverse cellular functions including cell morphology, migration, endocytosis and cell cycle progression. This protein is highly similar to Saccharomyces cerevisiae CDC 42, and is able to complement the yeast cdc42-1 mutant. The product of oncogene Dbl was reported to specifically catalyze the dissociation of GDP from this protein. This protein could regulate actin polymerization through its direct binding to Neural Wiskott-Aldrich syndrome protein (N-WASP), which subsequently activates Arp2/3 complex. Alternative splicing of this gene results in multiple transcript variants. Pseudogenes of this gene have been identified on chromosomes 3, 4, 5, 7, 8 and 20. [provided by RefSeq, Apr 2013]

CDC42 Products (3)

mRNA Protein Name
NM_001039802.2 NP_001034891.1 cell division control protein 42 homolog isoform 1 precursor
NM_001791.4 NP_001782.1 cell division control protein 42 homolog isoform 1 precursor
NM_044472.3 NP_426359.1 cell division control protein 42 homolog isoform 2
Molecular Function GO Annotation Evidence Verweise Source
enables GBD domain binding IPI
IPI: Inferred from physical interaction
8625410 GOA
enables GTP binding IDA
IDA: Inferred from direct assay
8625410 GOA
enables GTPase activity IDA
IDA: Inferred from direct assay
19787194 GOA
enables apolipoprotein A-I receptor binding IPI
IPI: Inferred from physical interaction
16443932 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
9748241 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
7493928 GOA
enables protein kinase binding IDA
IDA: Inferred from direct assay
19039103 GOA
enables protein kinase binding IPI
IPI: Inferred from physical interaction
8625410 GOA
enables thioesterase binding IPI
IPI: Inferred from physical interaction
12612085 GOA
enables ubiquitin protein ligase activity IDA
IDA: Inferred from direct assay
21435037 GOA
Biological Process GO Annotation Evidence Verweise Source
involved in actin cytoskeleton organization IDA
IDA: Inferred from direct assay
11035016 GOA
involved in actin filament organization IMP
IMP: Inferred from mutant phenotype
26465210 GOA
involved in cell junction assembly IMP
IMP: Inferred from mutant phenotype
22891260 GOA
involved in establishment of epithelial cell apical/basal polarity IMP
IMP: Inferred from mutant phenotype
22891260 GOA
involved in integrin-mediated signaling pathway IMP
IMP: Inferred from mutant phenotype
26051942 GOA
involved in modulation by host of viral process IMP
IMP: Inferred from mutant phenotype
19376974 GOA
involved in negative regulation of protein-containing complex assembly IPI
IPI: Inferred from physical interaction
11584266 GOA
involved in neuropilin signaling pathway IMP
IMP: Inferred from mutant phenotype
26051942 GOA
involved in phagocytosis, engulfment IMP
IMP: Inferred from mutant phenotype
26465210 GOA
involved in positive regulation of cell growth IMP
IMP: Inferred from mutant phenotype
21435037 GOA
involved in positive regulation of cell migration IMP
IMP: Inferred from mutant phenotype
20023705 GOA
involved in positive regulation of cytokinesis IMP
IMP: Inferred from mutant phenotype
15642749 GOA
involved in positive regulation of filopodium assembly IMP
IMP: Inferred from mutant phenotype
26051942 GOA
involved in positive regulation of lamellipodium assembly IMP
IMP: Inferred from mutant phenotype
8625410 GOA
involved in positive regulation of pseudopodium assembly IDA
IDA: Inferred from direct assay
11035016 GOA
involved in positive regulation of stress fiber assembly IMP
IMP: Inferred from mutant phenotype
8625410 GOA
involved in positive regulation of substrate adhesion-dependent cell spreading IDA
IDA: Inferred from direct assay
11807099 GOA
involved in regulation of actin cytoskeleton organization IMP
IMP: Inferred from mutant phenotype
26051942 GOA
involved in regulation of attachment of spindle microtubules to kinetochore IMP
IMP: Inferred from mutant phenotype
15642749 GOA
involved in regulation of filopodium assembly IDA
IDA: Inferred from direct assay
14978216 GOA
involved in regulation of lamellipodium assembly IGI
IGI: Inferred from genetic interaction
8625410 GOA
involved in regulation of stress fiber assembly IGI
IGI: Inferred from genetic interaction
8625410 GOA
Cellular Component GO Annotation Evidence Verweise Source
part of Golgi transport complex IMP
IMP: Inferred from mutant phenotype
16380373 GOA
colocalizes with centrosome IDA
IDA: Inferred from direct assay
20873783 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
11260256 GOA
located in cytoplasmic ribonucleoprotein granule IDA
IDA: Inferred from direct assay
15121898 GOA
located in filopodium IDA
IDA: Inferred from direct assay
11035016 GOA
located in membrane IDA
IDA: Inferred from direct assay
11807099 GOA
located in membrane IMP
IMP: Inferred from mutant phenotype
22801373 GOA
located in midbody IDA
IDA: Inferred from direct assay
15642749 GOA
located in mitotic spindle IDA
IDA: Inferred from direct assay
15642749 GOA
located in neuron projection IDA
IDA: Inferred from direct assay
21048939 GOA
located in neuronal cell body IDA
IDA: Inferred from direct assay
21048939 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
11260256 GOA
part of protein-containing complex IDA
IDA: Inferred from direct assay
20873783 GOA
located in spindle midzone IDA
IDA: Inferred from direct assay
15642749 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

CDC42 Protein Structure

Ras

Ras: Ras family (5 - 175)

  • 0
  • 100
  • 191 a.a.
Protein Preferred Names Protein Names

cell division control protein 42 homolog

  • G25K GTP-binding protein

CDC42 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
CDC42 P60953 PAK2 Homo sapiens Q13177 20936779
Intra
CDC42 P60953 PAK2 Homo sapiens Q13177 25416956
Intra
CDC42 P60953 PAK2 Homo sapiens Q13177 32296183
Intra
CDC42 P60953 PAK2 Homo sapiens Q13177 25416956
Intra
CDC42 P60953 PAK6 Homo sapiens Q9NQU5 31980649
Intra
CDC42 P60953 CDC42EP1 Homo sapiens Q00587-2 32296183
Intra
CDC42 P60953 CDC42EP1 Homo sapiens Q00587-2 32296183
Intra
CDC42 P60953 CDC42EP1 Homo sapiens Q00587-2 32296183
Cross
CDC42 P60953 sopB Salmonella typhimurium O30916 21435037
Intra
CDC42 P60953 HDAC7 Homo sapiens Q8WUI4-6 32296183
Intra
CDC42 P60953 PAK1 Homo sapiens Q13153 8107774
Intra
CDC42 P60953 PAK1 Homo sapiens Q13153 19596003
Intra
CDC42 P60953 PAK1 Homo sapiens Q13153 20936779
Intra
CDC42 P60953 PRKCI Homo sapiens P41743 14676191
Intra
CDC42 P60953 PRKCI Homo sapiens P41743
Y2H
11260256
Intra
CDC42 P60953 PRKCI Homo sapiens P41743 11260256
Intra
CDC42 P60953 PARD6B Homo sapiens Q9BYG5 32296183
Intra
CDC42 P60953 PARD6B Homo sapiens Q9BYG5 11260256
Intra
CDC42 P60953 PARD6B Homo sapiens Q9BYG5 11260256
Intra
CDC42 P60953 PARD6B Homo sapiens Q9BYG5 32296183
Intra
CDC42 P60953 PARD6B Homo sapiens Q9BYG5 25416956
Intra
CDC42 P60953 PARD6B Homo sapiens Q9BYG5 32296183
Intra
CDC42 P60953 PARD6B Homo sapiens Q9BYG5
Y2H
11260256
Intra
CDC42 P60953 PARD6B Homo sapiens Q9BYG5 14676191
Intra
CDC42 P60953 PARD6G Homo sapiens Q9BYG4
Y2H
11260256
Intra
CDC42 P60953 PARD6G Homo sapiens Q9BYG4 14676191
Intra
CDC42 P60953 PARD6G Homo sapiens Q9BYG4 11260256
Intra
CDC42 P60953 IQGAP1 Homo sapiens P46940 8670801
Intra
CDC42 P60953 IQGAP1 Homo sapiens P46940 8702968
Intra
CDC42 P60953 IQGAP1 Homo sapiens P46940 35271311
Intra
CDC42 P60953 IQGAP1 Homo sapiens P46940 8798539
Intra
CDC42 P60953 IQGAP1 Homo sapiens P46940 31980649
Intra
CDC42 P60953 IQGAP1 Homo sapiens P46940 8670801
Intra
CDC42 P60953 IQGAP1 Homo sapiens P46940 8798539
Intra
CDC42 P60953 IQGAP1 Homo sapiens P46940 26496610
Intra
CDC42 P60953 IQGAP1 Homo sapiens P46940
IF
18809683
Intra
CDC42 P60953 CDC42EP2 Homo sapiens O14613 32296183
Intra
CDC42 P60953 CDC42EP2 Homo sapiens O14613 25416956
Intra
CDC42 P60953 CDC42EP2 Homo sapiens O14613 32296183
Intra
CDC42 P60953 CDC42EP2 Homo sapiens O14613 20936779
Intra
CDC42 P60953 CDC42EP2 Homo sapiens O14613 25416956
Intra
CDC42 P60953 WAS Homo sapiens P42768
Y2H
22252508
Intra
CDC42 P60953 WAS Homo sapiens P42768 31515488
Intra
CDC42 P60953 WAS Homo sapiens P42768 25502805
Intra
CDC42 P60953 WAS Homo sapiens P42768 8625410
Intra
CDC42 P60953 WAS Homo sapiens P42768
SPR
9660763
Intra
CDC42 P60953 RIT1 Homo sapiens Q92963 29734338
Cross
CDC42 P60953 Pak3 Mus musculus Q61036 23022564
Intra
CDC42 P60953 BAIAP2 Homo sapiens Q9UQB8 21311754
Intra
CDC42 P60953 LRRK2 Homo sapiens Q5S007 21454543
Intra
CDC42 P60953 BAIAP2 Homo sapiens Q9UQB8-4 19171758
Intra
CDC42 P60953 BAIAP2 Homo sapiens Q9UQB8-4 24076653
Intra
CDC42 P60953 CDC42BPA Homo sapiens Q5VT25 15194684
Intra
CDC42 P60953 CDC42BPA Homo sapiens Q5VT25 35271311
Intra
CDC42 P60953 ARHGDIA Homo sapiens P52565 31980649
Intra
CDC42 P60953 PAK4 Homo sapiens O96013 22653441
Intra
CDC42 P60953 PAK4 Homo sapiens O96013 20936779
Intra
CDC42 P60953 PAK4 Homo sapiens O96013 29734338
Intra
CDC42 P60953 APC Homo sapiens P25054 21311754
Intra
CDC42 P60953 APC Homo sapiens P25054 21311754
Intra
CDC42 P60953 APC Homo sapiens P25054 21311754
Intra
CDC42 P60953 PAK5 Homo sapiens Q9P286 32296183
Intra
CDC42 P60953 PAK5 Homo sapiens Q9P286 32296183
Intra
CDC42 P60953 PAK5 Homo sapiens Q9P286 32296183
Intra
CDC42 P60953 CDC42EP1 Homo sapiens Q00587 25416956
Intra
CDC42 P60953 CDC42EP1 Homo sapiens Q00587 25416956
Intra
CDC42 P60953 CDC42EP1 Homo sapiens Q00587 16189514
Intra
CDC42 P60953 CDC42EP1 Homo sapiens Q00587 31980649
Intra
CDC42 P60953 CDC42EP1 Homo sapiens Q00587 35271311
Intra
CDC42 P60953 CDC42EP1 Homo sapiens Q00587
Y2H
21988832
Intra
CDC42 P60953 ABCA1 Homo sapiens O95477 16443932
Intra
CDC42 P60953 ABCA1 Homo sapiens O95477 16443932
Cross
CDC42 P60953 Pard6b Mus musculus Q9JK83 12606577
Cross
CDC42 P60953 Pard6b Mus musculus Q9JK83
Y2H
10934474
Cross
CDC42 P60953 Pard6b Mus musculus Q9JK83 10934474
Cross
CDC42 P60953 Pard6b Mus musculus Q9JK83 12606577
Intra
CDC42 P60953 PARD6A Homo sapiens Q9NPB6
Y2H
10934474
Intra
CDC42 P60953 PARD6A Homo sapiens Q9NPB6 14676191
Intra
CDC42 P60953 PARD6A Homo sapiens Q9NPB6
Y2H
11260256
Intra
CDC42 P60953 WASL Homo sapiens O00401 20936779
Cross
CDC42 P60953 Bin1 Drosophila melanogaster Q9VEX9
Y2H
9082982
Cross
CDC42 P60953 Bin1 Drosophila melanogaster Q9VEX9 9082982
Cross
CDC42 P60953 Wasl Rattus norvegicus O08816 9422512
Cross: Cross-species interaction Intra: Intraspecies interaction

CDC42 Antibodies

Art. -Nr. Produktname Anwendung Reactivity
HY-P82859 Phospho-Rac1/CDC42 (Ser71) Antibody (YA2604) WB Human
HY-P83703 CDC42 Antibody (YA3440) WB, ICC/IF, FC Human, Mouse, Rat

Related Diseases

Diseases Alias
Takenouchi-Kosaki Syndrome
  • Macrothrombocytopenia-Lymphedema-Developmental Delay-Facial Dysmorphism-Camptodactyly Syndrome

  • TKS

  • Macrothrombocytopenia And Mental Retardation Syndrome

Neonatal-Onset Severe Multisystemic Autoinflammatory Disease With Increased Il18
  • Neonatal-Onset Autoinflammation-Cytopenia-Facial Dysmorphism Syndrome

  • Neonatal-Onset Severe Multisystemic Autoinflammatory Disease With Increased Interleukin 18

Immune System Disease
  • Abnormality Of The Immune System

  • Immune System And Disorders

  • Immune System Diseases

Wiskott-Aldrich Syndrome
  • WAS

  • Eczema-Thrombocytopenia-Immunodeficiency Syndrome

  • Immunodeficiency 2

  • Aldrich Syndrome

  • Imd2

  • Wiskott-Aldrich Syndrome 1

  • Was1

  • Wiskott Syndrome

  • Wiskott Aldrich Syndrome

  • Eczema Thrombocytopenia Immunodeficiency Syndrome

  • Imd 2

Temperature-Sensitive Lethal Mutation
Aarskog-Scott Syndrome
  • Aarskog Syndrome

  • Faciogenital Dysplasia

  • Faciodigitogenital Syndrome

  • AAS

  • Fgdy

  • X-Linked Aarskog Syndrome

  • Intellectual Developmental Disorder, X-Linked, Syndromic 16

  • Aarskog Syndrome, X-Linked

  • Intellectual Developmental Disorder, X-Linked Syndromic 16

  • Greig'S Syndrome

  • Aarskog Scott Syndrome

  • Aarskog Disease

  • Scott Aarskog Syndrome

  • Facio-Digito-Genital Dysplasia

  • Faciogenital Dysplasia With Attention Deficit-Hyperactivity Disorder

  • Aarskog-Scott Syndrome ) Syndrome

Clostridium Difficile Colitis
  • Pseudomembranous Colitis

  • Colitis Pseudomembranous

  • Enterocolitis, Pseudomembranous

  • Pseudomembranous Enterocolitis

  • Clostridium Difficile Infection

Immunodeficiency 73a With Defective Neutrophil Chemotaxis And Leukocytosis
  • Neutrophil Immunodeficiency Syndrome

  • IMD73A

  • Immunodeficiency 73a With Defective Neutrophil Chemotaxix And Leukocytosis

  • Immunodeficiency, Type 73a, With Defective Neutrophil Chemotaxix And Leukocytosis

  • Rac 2 Deficiency

Charcot-Marie-Tooth Disease, Type 4h
  • Charcot-Marie-Tooth Disease Type 4h

  • CMT4H

  • Charcot-Marie-Tooth Neuropathy Type 4h

  • Charcot-Marie-Tooth Disease, Autosomal Recessive, Type 4h

  • Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive, Type 4h

  • Charcot-Marie-Tooth Neuropathy, Type 4h

  • Autosomal Recessive Charcot-Marie-Tooth Disease Type 4h

  • Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease Type 4h

  • Charcot-Marie-Tooth Disease 4h

  • Charcot-Marie-Tooth Disease Demyelinating Autosomal Recessive 4h

Unilateral Focal Polymicrogyria
Adams-Oliver Syndrome
  • Adams Oliver Syndrome

  • Aos

  • Congenital Scalp Defects With Distal Limb Reduction Anomalies

  • Aplasia Cutis Congenita With Terminal Transverse Limb Defects

  • Congenital Scalp Defects With Distal Limb Anomalies

  • Limb, Scalp And Skull Defects

  • Limb Scalp And Skull Defects

  • Absence Defect Of Limbs, Scalp, And Skull

Pancytopenia
Lissencephaly
  • Pachygyria

  • Broad Gyri Of Cerebrum

  • Large Gyri Of Cerebrum

  • Macrogyria

Breast Cancer
  • Breast Carcinoma

  • Male Breast Cancer

  • Breast Cancer, Familial

  • Malignant Neoplasm Of Breast

  • Breast Cancer, Susceptibility To

  • Breast Cancer, Early-Onset

  • Malignant Tumor Of Breast

  • Carcinoma Of Male Breast

  • Breast Cancer, Invasive Ductal

  • Breast Cancer, Protection Against

  • Breast Cancer, Somatic

  • Breast Cancer, Male

  • Breast Cancer, Lobular, Somatic

  • Breast Tumor

  • Mammary Cancer

  • Mammary Tumor

  • Malignant Neoplasm Of Male Breast

  • Mammary Carcinoma

  • Male Breast Carcinoma

  • Familial Cancer Of Breast

  • Invasive Ductal Breast Carcinoma

  • Breast Cancer Susceptibility

  • Breast Cancer, Male, Susceptibility To

  • Breast Cancer, Early-Onset, Susceptibility To

  • Malignant Tumor Of The Breast

  • Mammary Neoplasm

  • Primary Breast Cancer

  • Neoplasm Of Male Breast

  • Carcinoma Of Breast

  • Breast Cancer In Men

  • Familial Breast Cancer

  • Cancer Of Breast

  • BC

  • Breast Cancer Familial

  • Breast Cancer Familial Male

  • Breast Cancer, Familial Male

  • Breast Male Carcinoma

  • Breast Neoplasms

  • Breast Neoplasms, Male

  • Mammary Tumors

  • Mammary Carcinomas

  • Cancer, Breast

  • Cancer, Breast, Susceptibility

  • Invasive Breast Ductal Carcinoma

  • Breast Neoplasm

  • Susceptibility To Breast Cancer

  • Mammary Neoplasms

  • Animal Mammary Neoplasms

  • Primary Malignant Neoplasm Of Breast

  • Infiltrating Ductal Carcinoma Of Breast

  • Infiltrating Duct Carcinoma Of Unspecified Site

  • Infiltrating Ductular Carcinoma Of Unspecified Site

  • Invasive Breast Carcinoma Of No Special Type

  • Microinvasive Carcinoma Of Breast

  • Carcinoma With Apocrine Differentiation

Glioblastoma
  • Glioblastoma Multiforme

  • Gbm

  • Adult Glioblastoma Multiforme

  • Grade Iv Adult Astrocytic Tumor

  • Primary Glioblastoma Multiforme

  • Spongioblastoma Multiforme

  • Adult Glioblastoma

  • Primary Glioblastoma

Constipation
Neutropenia, Severe Congenital, X-Linked
  • X-Linked Severe Congenital Neutropenia

  • XLN

  • SCNX

  • Severe Congenital Neutropenia X-Linked

  • Neutropenia, Congenital, Severe, X-Linked

Asbestos-Related Lung Carcinoma
Colorectal Cancer
  • Colon Cancer

  • Colorectal Carcinoma

  • Colon Carcinoma

  • Colorectal Cancer, Susceptibility To

  • Carcinoma Of Colon

  • CRC

  • Colorectal Cancer With Chromosomal Instability, Somatic

  • Colon Cancer, Somatic

  • Colon Cancer, Susceptibility To

  • Colonic Neoplasms

  • Colorectal Neoplasms

  • Colorectal Cancer, Somatic

  • Colon Cancer, Advanced, Somatic

  • Colonic Carcinoma

  • Colorectal Carcinomas

  • Colon Cancers

  • Colorectal Cancers

  • Cancer, Colorectal, Somatic

  • Cancer, Colon

  • Cancer, Colorectal, Susceptibility To

  • Colorectal Neoplasm

  • Colonic Neoplasm

  • Malignant Tumor Of Colon

Lung Cancer
  • Lung Carcinoma

  • Non-Small Cell Lung Carcinoma

  • Lung Cancer, Susceptibility To

  • Lung Cancer, Protection Against

  • Adenocarcinoma Of Lung, Somatic

  • Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

  • Nonsmall Cell Lung Cancer

  • Lung Neoplasm

  • Carcinoma Of Lung

  • Lung Non-Small Cell Carcinoma

  • Non-Small Cell Lung Cancer

  • Nsclc

  • Lung Neoplasms

  • Malignant Neoplasm Of Lung

  • Alveolar Cell Carcinoma

  • Nonsmall Cell Lung Cancer, Somatic

  • Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

  • Nonsmall Cell Lung Cancer, Susceptibility To

  • Lung Cancer, Somatic

  • Lung Cancer, Resistance To

  • Cancer Of Lung

  • Cancer Of Bronchus

  • Cancer Of The Lung

  • Lung Malignancies

  • Lung Malignant Tumors

  • Malignant Lung Tumor

  • Malignant Tumor Of Lung

  • Pulmonary Cancer

  • Pulmonary Carcinoma

  • Pulmonary Neoplasms

  • Respiratory Carcinoma

  • LNCR

  • Adenocarcinoma Of Lung

  • Neoplasm Of Lung

  • Cancer Lung

  • Carcinoma Non-Small Cell Lung

  • Carcinoma, Non-Small-Cell Lung

  • Lung Cancers

  • Lung Carcinomas

  • Cancer, Lung

  • Cancer, Lung, Non-Small Cell

  • Primary Malignant Neoplasm Of Lung

  • Bronchioloalveolar Adenocarcinoma

Pheochromocytoma
  • Pheochromocytoma, Susceptibility To

  • Phaeochromocytoma

  • Adrenal Gland Chromaffin Paraganglioma

  • Adrenal Gland Chromaffinoma

  • Adrenal Gland Paraganglioma

  • Adrenal Gland Pheochromocytoma

  • Chromaffin Paraganglioma Of The Adrenal Gland

  • Intraadrenal Paraganglioma

  • PCC

  • Chromaffin Cell Tumor

  • Medullary Chromaffinoma

  • Medullary Paraganglioma

  • Pheochromoblastoma

  • Pheochromocytomas

  • Chromaffin Cell Neoplasm

  • Pheochromocytoma, Malignant

Spinal Cord Lipoma
  • Lipoma Of Spinal Cord

Thrombocytopenia
  • Low Platelet Count

  • Low Platelets

  • Decreased Platelets

  • Platelet Dysfunction Nos

Gastric Cancer
  • Stomach Cancer

  • Gastric Carcinoma

  • Stomach Carcinoma

  • Gastric Cancer, Somatic

  • Gastric Neoplasm

  • Carcinoma Of Stomach

  • Stomach Neoplasms

  • Malignant Neoplasm Of Stomach

  • Gastric Cancer Risk After H. Pylori Infection

  • Cancer Of The Stomach

  • Adult Stomach Cancer

  • Adult Stomach Carcinoma

  • GASC

  • Gastric Cancer Intestinal

  • Gastric Cancers

  • Gastric Carcinomas

  • Cancer, Gastric

  • Stomach Neoplasm

  • Malignant Neoplasm Of Body Of Stomach

  • Malignant Tumor Of Lesser Curve Of Stomach

  • Gastrocarcinoma Of Unspecified Site

  • Leather Bottle Stomach

  • Carcinoma Of Fundus Of Stomach

  • Cancer Of Fundus Of Stomach

  • Primary Malignant Neoplasm Of Body Of Stomach

  • Cancer Of Body Of Stomach

  • Primary Malignant Neoplasm Of Pyloric Antrum

  • Pyloric Antrum Cancer

  • Malignant Tumour Of Stomach

Salmonellosis
  • Salmonella Infections

  • Salmonella Infection

Neuroblastoma
  • Nb

  • Neuroblastoma, Susceptibility To

  • Neuroblastomas

  • Central Neuroblastoma

Ovarian Cancer
  • Ovarian Carcinoma

  • Ovarian Neoplasm

  • Malignant Tumour Of Ovary

  • Cancer Of The Ovary

  • Epithelial Ovarian Cancer

  • Neoplasm Of Ovary

  • Ovarian Neoplasms

  • Ovarian Cancers

  • Malignant Neoplasm Of Ovary

  • Primary Malignant Neoplasm Of Ovary

  • Ovarian Cancer, Somatic

  • Malignant Ovarian Tumor

  • Ovary Neoplasm

  • Primary Ovarian Cancer

  • Tumor Of The Ovary

  • Malignant Neoplasm Of The Ovary

  • Malignant Tumor Of The Ovary

  • Ovarian Malignant Tumor

  • OC

  • Ovarian Carcinomas

  • Cancer, Ovarian

  • Cancer Of Ovary

  • Ovary Cancer

  • Ca Ovary

Parameningeal Embryonal Rhabdomyosarcoma
Prolapse Of Urethra
  • Urethrocele

Periventricular Nodular Heterotopia
  • Periventricular Heterotopia

  • Pvnh

  • Familial Nodular Heterotopia

  • Heterotopia, Periventricular

  • Periventricular Heterotopia, X-Linked

Rasopathy
  • Ras/Mitogen-Activated Protein Kinase Syndrome

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

Congenital Nervous System Abnormality
  • Congenital Neurologic Anomaly

  • Congenital Nervous System Disorder

Peripheral Nervous System Disease
  • Peripheral Neuropathy

  • Peripheral Nerve Disease

  • Peripheral Nerve Disorders

  • Neuropathy, Peripheral

  • Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation

Nervous System Disease
  • Abnormality Of The Nervous System

  • Nervous System Diseases

  • Nervous System Disorder

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

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
Bos taurus CDC42 VGNC VGNC:97251
Rattus norvegicus CDC42 RGD RGD:71043
Mus musculus CDC42 MGD MGI:106211
Macaca mulatta CDC42 VGNC VGNC:106339
Others CDC42 NCBI