Airway smooth muscle cell contraction

No Pathway Network information available for Airway smooth muscle cell contraction

Pathways in the Airway smooth muscle cell contraction SuperPath

#	Name	Source	Genes
1	Airway smooth muscle cell contraction	WikiPathways	ADRB2 CD38 GDI1 GNAQ ITPR3 LOC105372522 MYL1 MYLK PPP1CB PPP1R14A RHOA ROCK1 ROCK2 RYR1 (see all 14) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	CD38	CD38 Molecule	Protein Coding	1
2	ROCK2	Rho Associated Coiled-Coil Containing Protein Kinase 2	Protein Coding	1
3	PPP1R14A	Protein Phosphatase 1 Regulatory Inhibitor Subunit 14A	Protein Coding	1
4	RYR1	Ryanodine Receptor 1	Protein Coding	1
5	ROCK1	Rho Associated Coiled-Coil Containing Protein Kinase 1	Protein Coding	1
6	MYLK	Myosin Light Chain Kinase	Protein Coding	1
7	MYL1	Myosin Light Chain 1	Protein Coding	1
8	RHOA	Ras Homolog Family Member A	Protein Coding	1
9	ITPR3	Inositol 1,4,5-Trisphosphate Receptor Type 3	Protein Coding	1
10	GNAQ	G Protein Subunit Alpha Q	Protein Coding	1
11	GDI1	GDP Dissociation Inhibitor 1	Protein Coding	1
12	ADRB2	Adrenoceptor Beta 2	Protein Coding	1
13	LOC105372522	Uncharacterized LOC105372522	RNA Gene	1
14	PPP1CB	Protein Phosphatase 1 Catalytic Subunit Beta	Protein Coding	1

Disorders associated with Airway smooth muscle cell contraction SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Sturge-weber syndrome	Enrichment	GNAQ	2.99
2	Charcot-marie-tooth disease, demyelinating, type 1j	Enrichment	ITPR3	2.99
3	Intellectual developmental disorder, x-linked 41	Enrichment	GDI1	2.99
4	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies	Enrichment	RHOA	2.99
5	Noonan syndrome-like disorder with loose anagen hair 2	Enrichment	PPP1CB	2.99
6	Congenital myopathy 14	Enrichment	MYL1	2.99
7	Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies	Enrichment	RHOA	2.99
8	Congenital myopathy with myasthenic-like onset	Enrichment	RYR1	2.99
9	Immunodeficiency 133 with ectodermal dysplasia with or without peripheral neuropathy	Enrichment	ITPR3	2.99
10	Calf-predominant weakness-gastrocnemius medialis atrophy-distal myopathy	Enrichment	RYR1	2.99
11	Benign samaritan congenital myopathy	Enrichment	RYR1	2.99
12	Malignant hyperthermia 1	Enrichment	RYR1	2.69
13	Noonan syndrome-like disorder with loose anagen hair	Enrichment	PPP1CB	2.69
14	King-denborough syndrome	Enrichment	RYR1	2.69
15	Exercise-induced malignant hyperthermia	Enrichment	RYR1	2.69
16	Phakomatosis cesioflammea	Enrichment	GNAQ	2.69
17	Aortic aneurysm, familial thoracic 7	Enrichment	MYLK	2.51
18	Lynch syndrome 5	Enrichment	RYR1	2.51
19	Bronchopulmonary dysplasia	Enrichment	RYR1	2.51
20	Anastomosing haemangioma	Enrichment	GNAQ	2.51
21	Congenital myopathy 1a, autosomal dominant, with malignant hyperthermia	Enrichment	RYR1	2.38
22	Megacystis-microcolon-intestinal hypoperistalsis syndrome 1	Enrichment	MYLK	2.38
23	Myopathy, centronuclear, 2	Enrichment	RYR1	2.38
24	Sacral defect with anterior meningocele	Enrichment	RYR1	2.38
25	Intellectual developmental disorder, autosomal dominant 26	Enrichment	RYR1	2.38
26	Congenital myopathy 1a	Enrichment	RYR1	2.38
27	Malignant hyperthermia	Enrichment	RYR1	2.38
28	Capillary malformations, congenital	Enrichment	GNAQ	2.29
29	Visceral myopathy 1	Enrichment	MYLK	2.29
30	Congenital myopathy 1b, autosomal recessive	Enrichment	RYR1	2.29
31	Klippel-trenaunay-weber syndrome	Enrichment	GNAQ	2.21
32	Melanoma, uveal	Enrichment	GNAQ	2.21
33	Myopathy, centronuclear, 1	Enrichment	RYR1	2.21
34	Hemihyperplasia, isolated	Enrichment	RHOA	2.21
35	Multiple pterygium syndrome, lethal type	Enrichment	RYR1	2.08
36	Congenital muscular dystrophy	Enrichment	RYR1	2.08
37	Familial thoracic aortic aneurysm and dissection	Enrichment	MYLK	2.03
38	Hydrops fetalis	Enrichment	RYR1	2.03
39	Congenital long qt syndrome	Enrichment	ITPR3	1.91
40	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly	Enrichment	RYR1	1.87
41	Clubfoot	Enrichment	RYR1	1.87
42	Aortic aneurysm, familial thoracic 1	Enrichment	MYLK	1.84
43	Congenital myopathy 4a, autosomal dominant	Enrichment	RYR1	1.81
44	Arrhythmogenic right ventricular cardiomyopathy	Enrichment	RYR1	1.79
45	Dandy-walker syndrome	Enrichment	PPP1CB	1.76
46	Beckwith-wiedemann syndrome	Enrichment	RYR1	1.73
47	Neuromuscular disease	Enrichment	RYR1	1.73
48	Congenital myopathy	Enrichment	RYR1	1.71
49	Centronuclear myopathy	Enrichment	RYR1	1.67
50	Noonan syndrome 1	Enrichment	PPP1CB	1.63
51	Scoliosis	Enrichment	RYR1	1.61
52	Rasopathy	Enrichment	PPP1CB	1.58
53	Long qt syndrome 1	Enrichment	ITPR3	1.52
54	Non-syndromic x-linked intellectual disability	Enrichment	GDI1	1.44
55	Fetal akinesia deformation sequence 1	Enrichment	RYR1	1.43
56	Myopathy	Enrichment	RYR1	1.39
57	Distal arthrogryposis	Enrichment	RYR1	1.37
58	Familial thoracic aortic aneurysm and aortic dissection	Enrichment	MYLK	1.35

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

Airway smooth muscle cell contraction

Pathway Network for Airway smooth muscle cell contraction

Member Pathways for Airway smooth muscle cell contraction

Pathways in the Airway smooth muscle cell contraction SuperPath

Associated Genes for Airway smooth muscle cell contraction

Associated Disorders for Airway smooth muscle cell contraction

Disorders associated with Airway smooth muscle cell contraction SuperPath

STRING Interaction Network for Airway smooth muscle cell contraction

Sources for Airway smooth muscle cell contraction