Salmonella Infection

No Pathway Network information available for Salmonella Infection

Pathways in the Salmonella Infection SuperPath

#	Name	Source	Genes
1	Salmonella Infection	QIAGEN	ACTA1 ACTA2 ACTB ACTG1 ACTG2 ACTR2 ACTR3 ARPC1B ARPC3 ARPC4 ARPC5 CCNH CDC42 MAPK1 MAPK10 MAPK11 MAPK12 MAPK13 MAPK14 MAPK3 MAPK6 MAPK7 MAPK8 MAPK9 RAC1 WAS WASF1 (see all 27) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	ACTA1	Actin Alpha 1, Skeletal Muscle	Protein Coding	1
2	ACTA2	Actin Alpha 2, Smooth Muscle	Protein Coding	1
3	ACTB	Actin Beta	Protein Coding	1
4	ACTG1	Actin Gamma 1	Protein Coding	1
5	ACTG2	Actin Gamma 2, Smooth Muscle	Protein Coding	1
6	ACTR2	Actin Related Protein 2	Protein Coding	1
7	ACTR3	Actin Related Protein 3	Protein Coding	1
8	ARPC1B	Actin Related Protein 2/3 Complex Subunit 1B	Protein Coding	1
9	ARPC3	Actin Related Protein 2/3 Complex Subunit 3	Protein Coding	1
10	ARPC4	Actin Related Protein 2/3 Complex Subunit 4	Protein Coding	1
11	ARPC5	Actin Related Protein 2/3 Complex Subunit 5	Protein Coding	1
12	CCNH	Cyclin H	Protein Coding	1
13	CDC42	Cell Division Cycle 42	Protein Coding	1
14	MAPK1	Mitogen-Activated Protein Kinase 1	Protein Coding	1
15	MAPK10	Mitogen-Activated Protein Kinase 10	Protein Coding	1
16	MAPK11	Mitogen-Activated Protein Kinase 11	Protein Coding	1
17	MAPK12	Mitogen-Activated Protein Kinase 12	Protein Coding	1
18	MAPK13	Mitogen-Activated Protein Kinase 13	Protein Coding	1
19	MAPK14	Mitogen-Activated Protein Kinase 14	Protein Coding	1
20	MAPK3	Mitogen-Activated Protein Kinase 3	Protein Coding	1
21	MAPK6	Mitogen-Activated Protein Kinase 6	Protein Coding	1
22	MAPK7	Mitogen-Activated Protein Kinase 7	Protein Coding	1
23	MAPK8	Mitogen-Activated Protein Kinase 8	Protein Coding	1
24	MAPK9	Mitogen-Activated Protein Kinase 9	Protein Coding	1
25	RAC1	Rac Family Small GTPase 1	Protein Coding	1
26	WAS	WASP Actin Nucleation Promoting Factor	Protein Coding	1
27	WASF1	WASP Family Member 1	Protein Coding	1

Disorders associated with Salmonella Infection SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Baraitser-winter cerebrofrontofacial syndrome	Enrichment	ACTB, ACTG1	5.42
2	Microcephaly	Enrichment	ACTB, ACTG1, MAPK1	2.74
3	Baraitser-winter syndrome 1	Enrichment	ACTB	2.70
4	Thrombocytopenia 1	Enrichment	WAS	2.70
5	Congenital myopathy 2a, typical, autosomal dominant	Enrichment	ACTA1	2.70
6	Myopathy, scapulohumeroperoneal	Enrichment	ACTA1	2.70
7	Megacystis-microcolon-intestinal hypoperistalsis syndrome 5	Enrichment	ACTG2	2.70
8	Neurodevelopmental disorder with absent language and variable seizures	Enrichment	WASF1	2.70
9	Noonan syndrome 13	Enrichment	MAPK1	2.70
10	Congenital smooth muscle hamartoma, with or without hemihypertrophy	Enrichment	ACTB	2.70
11	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia	Enrichment	ARPC1B	2.70
12	Becker nevus syndrome	Enrichment	ACTB	2.70
13	Dystonia-deafness syndrome 1	Enrichment	ACTB	2.70
14	Visceral neuropathy, familial, 3, autosomal dominant	Enrichment	ACTG2	2.70
15	Congenital myopathy 2b, severe infantile, autosomal recessive	Enrichment	ACTA1	2.70
16	Autosomal dominant familial visceral neuropathy	Enrichment	ACTG2	2.70
17	Was-related disorders	Enrichment	WAS	2.70
18	Takenouchi-kosaki syndrome	Enrichment	CDC42	2.70
19	Congenital myopathy 2c, severe infantile, autosomal dominant	Enrichment	ACTA1	2.70
20	Thrombocytopenia 8, with dysmorphic features and developmental delay	Enrichment	ACTB	2.70
21	Baraitser-winter syndrome	Enrichment	ACTB	2.70
22	Zebra body myopathy	Enrichment	ACTA1	2.70
23	Congenital smooth muscle hamartoma	Enrichment	ACTB	2.70
24	Nocarh syndrome	Enrichment	CDC42	2.70
25	Developmental malformations-deafness-dystonia syndrome	Enrichment	ACTB	2.70
26	Actin-accumulation myopathy	Enrichment	ACTA1	2.70
27	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom	Enrichment	RAC1	2.70
28	Myopathic intestinal pseudoobstruction	Enrichment	ACTG2	2.70
29	Actg2 visceral myopathy	Enrichment	ACTG2	2.70
30	Scoliosis, isolated 1	Enrichment	MAPK7	2.40
31	Neutropenia, severe congenital, x-linked	Enrichment	WAS	2.40
32	Wiskott-aldrich syndrome	Enrichment	WAS	2.40
33	Aortic aneurysm, familial thoracic 2	Enrichment	ACTA2	2.40
34	Deafness, autosomal dominant 20	Enrichment	ACTG1	2.40
35	Smooth muscle dysfunction syndrome	Enrichment	ACTA2	2.40
36	Aortic aneurysm, familial thoracic 6	Enrichment	ACTA2	2.40
37	Baraitser-winter syndrome 2	Enrichment	ACTG1	2.40
38	Moyamoya disease 5	Enrichment	ACTA2	2.40
39	Intellectual developmental disorder, autosomal dominant 48	Enrichment	RAC1	2.40
40	Developmental delay, language impairment, and ocular abnormalities	Enrichment	ARPC4	2.40
41	Immunodeficiency 113 with autoimmunity and autoinflammation	Enrichment	ARPC5	2.40
42	Immune system disease	Enrichment	CDC42	2.40
43	Immunodeficiency 133	Enrichment	ARPC5	2.40
44	Intestinal obstruction	Enrichment	ACTG2	2.40
45	Wieacker-wolff syndrome	Enrichment	CCNH	2.22
46	Nemaline myopathy 2	Enrichment	ACTA1	2.10
47	Megacystis-microcolon-intestinal hypoperistalsis syndrome 1	Enrichment	ACTG2	2.10
48	Autoimmune lymphoproliferative syndrome	Enrichment	ACTA2	2.10
49	Chromosome 22q11.2 deletion syndrome, distal	Enrichment	MAPK1	2.10
50	Aminoacylase 1 deficiency	Enrichment	ACTB	2.10
51	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia	Enrichment	CDC42	2.10
52	Intermediate nemaline myopathy	Enrichment	ACTA1	2.10
53	Pseudomyogenic hemangioendothelioma	Enrichment	ACTB	2.10
54	Capillary malformations, congenital	Enrichment	CCNH	2.00
55	Visceral myopathy 1	Enrichment	ACTG2	2.00
56	Congenital myopathy 3 with rigid spine	Enrichment	ACTA1	2.00
57	Coloboma of choroid and retina	Enrichment	ACTG1	2.00
58	Severe congenital nemaline myopathy	Enrichment	ACTA1	2.00
59	Klippel-trenaunay-weber syndrome	Enrichment	CCNH	1.92
60	Telangiectasia, hereditary hemorrhagic, type 1	Enrichment	CCNH	1.92
61	Moyamoya disease 1	Enrichment	ACTA2	1.92
62	Hemangioma, capillary infantile	Enrichment	CCNH	1.92
63	Basal cell carcinoma 1	Enrichment	CCNH	1.92
64	Intestinal pseudo-obstruction	Enrichment	ACTG2	1.92
65	Typical nemaline myopathy	Enrichment	ACTA1	1.92
66	Capillary malformation-arteriovenous malformation 1	Enrichment	CCNH	1.86
67	Hereditary hemorrhagic telangiectasia	Enrichment	CCNH	1.86
68	Childhood-onset nemaline myopathy	Enrichment	ACTA1	1.86
69	Lennox-gastaut syndrome	Enrichment	MAPK10	1.80
70	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies	Enrichment	RAC1	1.75
71	Arteriovenous malformation	Enrichment	CCNH	1.75
72	Cat eye syndrome	Enrichment	ACTG1	1.70
73	Myopathy, x-linked, with excessive autophagy	Enrichment	CCNH	1.70
74	Nemaline myopathy	Enrichment	ACTA1	1.70
75	Combined immunodeficiency	Enrichment	ARPC1B	1.66
76	Combined t cell and b cell immunodeficiency	Enrichment	ARPC1B	1.66
77	Specific learning disability	Enrichment	MAPK1	1.66
78	Combined t and b cell immunodeficiency	Enrichment	ARPC1B	1.66
79	Lung cancer susceptibility 3	Enrichment	ACTA2	1.56
80	Congenital myopathy 4a, autosomal dominant	Enrichment	ACTA1	1.53
81	Heart, malformation of	Enrichment	MAPK1	1.45
82	Neuromuscular disease	Enrichment	ACTA1	1.45
83	Congenital myopathy	Enrichment	ACTA1	1.43
84	Lissencephaly	Enrichment	ACTG1	1.39
85	Centronuclear myopathy	Enrichment	ACTA1	1.39
86	Hydrops fetalis, nonimmune	Enrichment	ACTA1	1.30
87	Non-immune hydrops fetalis	Enrichment	ACTA1	1.22
88	Lung cancer	Enrichment	ACTA2	1.21
89	Connective tissue disease	Enrichment	ACTA2	1.21
90	Cakut	Enrichment	ACTG1	1.18
91	Non-syndromic genetic deafness	Enrichment	ACTG1	1.16
92	Fetal akinesia deformation sequence 1	Enrichment	ACTA1	1.15
93	Myopathy	Enrichment	ACTA1	1.12
94	Distal arthrogryposis	Enrichment	ACTA1	1.09
95	Nonsyndromic hearing loss	Enrichment	ACTG1	1.09
96	Familial thoracic aortic aneurysm and aortic dissection	Enrichment	ACTA2	1.08
97	Thrombocytopenia	Enrichment	WAS	1.04
98	Rare autosomal dominant non-syndromic sensorineural deafness type dfna	Enrichment	ACTG1	1.01
99	Rare genetic deafness	Enrichment	ACTG1	0.84
100	Dilated cardiomyopathy	Enrichment	ACTA1	0.83
101	Complex neurodevelopmental disorder	Enrichment	WASF1	0.66

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

Salmonella Infection

Pathway Network for Salmonella Infection

Member Pathways for Salmonella Infection

Pathways in the Salmonella Infection SuperPath

Associated Genes for Salmonella Infection

Associated Disorders for Salmonella Infection

Disorders associated with Salmonella Infection SuperPath

STRING Interaction Network for Salmonella Infection

Sources for Salmonella Infection