RHOBTB3 ATPase cycle

No Pathway Network information available for RHOBTB3 ATPase cycle

Pathways in the RHOBTB3 ATPase cycle SuperPath

#	Name	Source	Genes
1	RHOBTB3 ATPase cycle	Reactome	CCNE1 CUL3 HGS HTR7 LRRC41 PLIN3 RAB9A RAB9B RHOBTB3 VHL (see all 10) (see less)

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

#	Symbol	Description	Category	# Related Pathways
1	PLIN3	Perilipin 3	Protein Coding	1
2	LRRC41	Leucine Rich Repeat Containing 41	Protein Coding	1
3	RHOBTB3	Rho Related BTB Domain Containing 3	Protein Coding	1
4	HTR7	5-Hydroxytryptamine Receptor 7	Protein Coding	1
5	RAB9B	RAB9B, Member RAS Oncogene Family	Protein Coding	1
6	VHL	Von Hippel-Lindau Tumor Suppressor	Protein Coding	1
7	CUL3	Cullin 3	Protein Coding	1
8	CCNE1	Cyclin E1	Protein Coding	1
9	HGS	Hepatocyte Growth Factor-Regulated Tyrosine Kinase Substrate	Protein Coding	1
10	RAB9A	RAB9A, Member RAS Oncogene Family	Protein Coding	1

Disorders associated with RHOBTB3 ATPase cycle SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Pseudohypoaldosteronism, type iie	Enrichment	CUL3	3.13
2	Neurodevelopmental disorder with or without autism or seizures	Enrichment	CUL3	3.13
3	Retinal hemangioblastoma	Enrichment	VHL	3.13
4	Pseudohypoaldosteronism, type i, autosomal dominant	Enrichment	CUL3	2.83
5	Acute leukemia of ambiguous lineage	Enrichment	VHL	2.83
6	Pseudohypoaldosteronism, type iia	Enrichment	CUL3	2.66
7	Myasthenic syndrome, congenital, 6, presynaptic	Enrichment	VHL	2.66
8	Pelizaeus-merzbacher disease	Enrichment	RAB9B	2.66
9	Spastic paraplegia 2, x-linked	Enrichment	RAB9B	2.66
10	Primary polycythemia	Enrichment	VHL	2.66
11	Pelizeaus-merzbacher spectrum disorder	Enrichment	RAB9B	2.66
12	Erythrocytosis, familial, 2	Enrichment	VHL	2.53
13	Au-kline syndrome	Enrichment	VHL	2.53
14	Fanconi anemia, complementation group d2	Enrichment	VHL	2.43
15	Von hippel-lindau syndrome	Enrichment	VHL	2.43
16	Sporadic pheochromocytoma/secreting paraganglioma	Enrichment	VHL	2.35
17	Renal cell carcinoma, papillary, 1	Enrichment	VHL	2.29
18	Multiple enchondromatosis, maffucci type	Enrichment	VHL	2.29
19	Nk-cell enteropathy	Enrichment	CUL3	2.02
20	Pheochromocytoma	Enrichment	VHL	1.99
21	Renal cell carcinoma, nonpapillary	Enrichment	VHL	1.96
22	Hereditary paraganglioma-pheochromocytoma syndromes	Enrichment	VHL	1.81
23	Auditory neuropathy	Enrichment	RAB9B	1.72
24	Fanconi anemia, complementation group a	Enrichment	VHL	1.59
25	Hereditary spastic paraplegia	Enrichment	RAB9B	1.52
26	Primary ovarian insufficiency	Enrichment	LRRC41	1.37
27	Autism spectrum disorder	Enrichment	CUL3	1.11
28	Complex neurodevelopmental disorder	Enrichment	CUL3	1.06
29	Inherited cancer-predisposing syndrome	Enrichment	VHL	1.03

¹ WikiPathways

² PubChem

³ R&D Systems

⁴ Reactome

⁵ GeneGo (Thomson Reuters)

⁶ QIAGEN

⁷ PharmGKB

⁸ Cell Signaling Technology

⁹ Sino Biological

¹⁰ Tocris

¹¹ MalaCards

RHOBTB3 ATPase cycle

Pathway Network for RHOBTB3 ATPase cycle

Member Pathways for RHOBTB3 ATPase cycle

Pathways in the RHOBTB3 ATPase cycle SuperPath

Associated Genes for RHOBTB3 ATPase cycle

Associated Disorders for RHOBTB3 ATPase cycle

Disorders associated with RHOBTB3 ATPase cycle SuperPath

STRING Interaction Network for RHOBTB3 ATPase cycle

Sources for RHOBTB3 ATPase cycle