Cardiomyocyte signaling pathways converging on Titin

No Pathway Network information available for Cardiomyocyte signaling pathways converging on Titin

Pathways in the Cardiomyocyte signaling pathways converging on Titin SuperPath

#	Name	Source	Genes
1	Cardiomyocyte signaling pathways converging on Titin	WikiPathways	ANKRD1 ANKRD2 ANKRD23 CAMK2A CSRP3 GUCD1 GUCY1B1 MAPK1 MYPN PRKAR1A PRKCA TCAP TTN (see all 13) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	TCAP	Titin-Cap	Protein Coding	1
2	MYPN	Myopalladin	Protein Coding	1
3	GUCD1	Guanylyl Cyclase Domain Containing 1	Protein Coding	1
4	CAMK2A	Calcium/Calmodulin Dependent Protein Kinase II Alpha	Protein Coding	1
5	CSRP3	Cysteine And Glycine Rich Protein 3	Protein Coding	1
6	TTN	Titin	Protein Coding	1
7	MAPK1	Mitogen-Activated Protein Kinase 1	Protein Coding	1
8	PRKCA	Protein Kinase C Alpha	Protein Coding	1
9	PRKAR1A	Protein Kinase CAMP-Dependent Type I Regulatory Subunit Alpha	Protein Coding	1
10	ANKRD1	Ankyrin Repeat Domain 1	Protein Coding	1
11	ANKRD23	Ankyrin Repeat Domain 23	Protein Coding	1
12	GUCY1B1	Guanylate Cyclase 1 Soluble Subunit Beta 1	Protein Coding	1
13	ANKRD2	Ankyrin Repeat Domain 2	Protein Coding	1

Disorders associated with Cardiomyocyte signaling pathways converging on Titin SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Familial isolated dilated cardiomyopathy	Enrichment	ANKRD1, CSRP3, MYPN, TCAP, TTN	9.02
2	Dilated cardiomyopathy	Enrichment	CSRP3, MYPN, TCAP, TTN	6.11
3	Hypertrophic cardiomyopathy	Enrichment	CSRP3, TCAP, TTN	5.08
4	Congenital myopathy	Enrichment	MYPN, TTN	3.84
5	Familial hypertrophic cardiomyopathy	Enrichment	CSRP3, TCAP	3.36
6	Acrodysostosis 1 with or without hormone resistance	Enrichment	PRKAR1A	3.02
7	Carney complex, type 1	Enrichment	PRKAR1A	3.02
8	Muscular dystrophy, limb-girdle, autosomal recessive 7	Enrichment	TCAP	3.02
9	Noonan syndrome 13	Enrichment	MAPK1	3.02
10	Intellectual developmental disorder, autosomal recessive 63	Enrichment	CAMK2A	3.02
11	Myxoma, intracardiac	Enrichment	PRKAR1A	3.02
12	Cardiomyopathy, familial hypertrophic, 12	Enrichment	CSRP3	3.02
13	Cardiomyopathy, dilated, 1m	Enrichment	CSRP3	3.02
14	Autosomal recessive limb-girdle muscular dystrophy type 2g	Enrichment	TCAP	3.02
15	Congenital myopathy 24	Enrichment	MYPN	3.02
16	Intellectual developmental disorder, autosomal dominant 53	Enrichment	CAMK2A	3.02
17	Childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome	Enrichment	TTN	3.02
18	Amelogenesis imperfecta, type ig	Enrichment	PRKAR1A	2.72
19	Pigmented nodular adrenocortical disease, primary, 1	Enrichment	PRKAR1A	2.72
20	Cardiomyopathy, familial hypertrophic, 25	Enrichment	TCAP	2.72
21	Cardiomyopathy, dilated, 1kk	Enrichment	MYPN	2.72
22	Usher syndrome, type iv	Enrichment	PRKAR1A	2.72
23	Acrodysostosis	Enrichment	PRKAR1A	2.72
24	Isolated primary pigmented nodular adrenocortical disease	Enrichment	PRKAR1A	2.72
25	Inclusion myopathy	Enrichment	TTN	2.72
26	Myopathy, myofibrillar, 1	Enrichment	TTN	2.54
27	Nonaka myopathy	Enrichment	TTN	2.54
28	Cap myopathy	Enrichment	MYPN	2.54
29	Myopathy, centronuclear, 2	Enrichment	TTN	2.42
30	Chromosome 22q11.2 deletion syndrome, distal	Enrichment	MAPK1	2.42
31	Carney complex variant	Enrichment	PRKAR1A	2.42
32	Left ventricular noncompaction 2	Enrichment	TTN	2.42
33	Arrhythmogenic right ventricular dysplasia, familial, 10	Enrichment	PRKAR1A	2.42
34	Feingold syndrome 1	Enrichment	TTN	2.32
35	Arrhythmogenic right ventricular dysplasia, familial, 1	Enrichment	TTN	2.32
36	Congenital myopathy 1b, autosomal recessive	Enrichment	TTN	2.32
37	Congenital myopathy 3 with rigid spine	Enrichment	TTN	2.32
38	Arrhythmogenic right ventricular dysplasia 1	Enrichment	TTN	2.32
39	Adrenocortical carcinoma	Enrichment	PRKAR1A	2.24
40	Third-degree atrioventricular block	Enrichment	TTN	2.17
41	Childhood-onset nemaline myopathy	Enrichment	MYPN	2.17
42	Familial isolated restrictive cardiomyopathy	Enrichment	MYPN	2.17
43	Orthostatic intolerance	Enrichment	TTN	2.12
44	Congenital muscular dystrophy	Enrichment	TTN	2.12
45	Myocarditis	Enrichment	TTN	2.12
46	Orofacial cleft 1	Enrichment	TTN	2.07
47	Arrhythmogenic right ventricular dysplasia, familial, 9	Enrichment	TTN	2.07
48	Limb-girdle muscular dystrophy	Enrichment	TTN	2.07
49	Tibial muscular dystrophy, tardive	Enrichment	TTN	2.02
50	Myopathy, myofibrillar, 9, with early respiratory failure	Enrichment	TTN	2.02
51	Tibial muscular dystrophy	Enrichment	TTN	2.02
52	Nemaline myopathy	Enrichment	MYPN	2.02
53	Cardiomyopathy, familial hypertrophic, 9	Enrichment	TTN	1.98
54	Specific learning disability	Enrichment	MAPK1	1.98
55	Restrictive cardiomyopathy	Enrichment	TTN	1.94
56	Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variant	Enrichment	TTN	1.94
57	Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variant	Enrichment	TTN	1.94
58	Congenital myopathy 5 with cardiomyopathy	Enrichment	TTN	1.91
59	Acute promyelocytic leukemia	Enrichment	PRKAR1A	1.91
60	Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant	Enrichment	TTN	1.87
61	Creatine phosphokinase, elevated serum	Enrichment	TCAP	1.82
62	Wolff-parkinson-white syndrome	Enrichment	TTN	1.82
63	Isolated elevated serum creatine phosphokinase levels	Enrichment	TCAP	1.82
64	Sudden infant death syndrome	Enrichment	TTN	1.79
65	Cardiomyopathy, dilated, 1e	Enrichment	TTN	1.79
66	Heart, malformation of	Enrichment	MAPK1	1.77
67	Neuromuscular disease	Enrichment	TTN	1.77
68	Muscular dystrophy, limb-girdle, autosomal recessive 10	Enrichment	TTN	1.74
69	Cardiomyopathy, dilated, 1a	Enrichment	TTN	1.70
70	Autosomal recessive limb-girdle muscular dystrophy type 2j	Enrichment	TTN	1.70
71	Centronuclear myopathy	Enrichment	TTN	1.70
72	Cardiomyopathy, dilated, 1g	Enrichment	TTN	1.68
73	Familial atrial fibrillation	Enrichment	TTN	1.64
74	Muscular dystrophy	Enrichment	TTN	1.64
75	Left ventricular noncompaction	Enrichment	TTN	1.48
76	Cerebral palsy	Enrichment	TTN	1.43
77	Myopathy	Enrichment	TTN	1.42
78	Autosomal dominant non-syndromic intellectual disability	Enrichment	CAMK2A	1.33
79	Microcephaly	Enrichment	MAPK1	0.95
80	Inherited cancer-predisposing syndrome	Enrichment	PRKAR1A	0.92

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

Cardiomyocyte signaling pathways converging on Titin

Pathway Network for Cardiomyocyte signaling pathways converging on Titin

Member Pathways for Cardiomyocyte signaling pathways converging on Titin

Pathways in the Cardiomyocyte signaling pathways converging on Titin SuperPath

Associated Genes for Cardiomyocyte signaling pathways converging on Titin

Associated Disorders for Cardiomyocyte signaling pathways converging on Titin

Disorders associated with Cardiomyocyte signaling pathways converging on Titin SuperPath

STRING Interaction Network for Cardiomyocyte signaling pathways converging on Titin

Sources for Cardiomyocyte signaling pathways converging on Titin