VEGFA-VEGFR2 signaling

No Pathway Network information available for VEGFA-VEGFR2 signaling

Pathways in the VEGFA-VEGFR2 signaling SuperPath

#	Name	Source	Genes
1	VEGFA-VEGFR2 signaling	WikiPathways	ABCF2 ACOT9 ACTG1 ALB ALDOA ANXA1 AP2A1 AP2S1 ARF4 ARMCX1 ARPC5L ASCC3 ATP6V0D1 ATP6V1E1 BSG CACNA2D1 CALR CALU CAPZB CCDC124 CCN1 CCT7 CDC42BPB CGNL1 CLIC1 CNP COPG1 CRIP2 CSRP1 CSRP2 DECR1 DHX29 DHX36 DNAJA1 DNAJB4 DPM1 DSC1 EIF3D EIF3F EIF3H EIF4G1 EIF4G2 ELOC EPB41 EPRS1 EWSR1 FAM120A FARSB FGD5 FHOD1 FLII FMNL3 FN1 FSCN1 FXR2 GAPDH GIGYF2 GLUD1 GRSF1 HBD HMGB1 HSP90AA1 HSP90AB2P HTRA1 HYOU1 IDH2 INPP5K IQGAP1 KANK1 KATNAL2 LDHA LMAN1 LRRC59 LRRFIP2 LUC7L MICAL2 MOV10 MYH11 MYO1C MYO6 NAP1L1 NAPA NCL NEXN NUMB OCRL P4HA2 P4HB PABPC1 PBXIP1 PDE4DIP PDIA6 PFN1 PGD PGK1 PLOD3 PPM1G PPP1CA PPP2CA PRDX2 PRDX6 PRKRA PRRC2C PSMD11 PSMD4 PTMA PTPN14 QKI RBM39 RCN1 RPL10A RPL13A RPL18A RPL26 RPL27 RPL39P5 RPL5 RPL7 RPLP2 RPS11 SARS1 SET SH3BGRL3 SHROOM2 SLC25A11 SND1 SPIRE1 SRP54 SRPK1 SSR3 SSR4 STIP1 SYNJ1 TAOK2 TBCA TFAM TFCP2 TKT TMOD1 TMOD3 TMSB10 TMSB4X TPM3 TPP1 TRIP4 TUBA1C TUBB8 TXNDC5 UBAP2L USP10 VPS39 YWHAE ZC3H15 (see all 153) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	ARF4	ARF GTPase 4	Protein Coding	1
2	MICAL2	Microtubule Associated Monooxygenase, Calponin And LIM Domain Containing 2	Protein Coding	1
3	PRDX6	Peroxiredoxin 6	Protein Coding	1
4	CDC42BPB	CDC42 Binding Protein Kinase Beta	Protein Coding	1
5	QKI	QKI, KH Domain Containing RNA Binding	Protein Coding	1
6	TRIP4	Thyroid Hormone Receptor Interactor 4	Protein Coding	1
7	TMSB10	Thymosin Beta 10	Protein Coding	1
8	NEXN	Nexilin F-Actin Binding Protein	Protein Coding	1
9	PLOD3	Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 3	Protein Coding	1
10	P4HA2	Prolyl 4-Hydroxylase Subunit Alpha 2	Protein Coding	1
11	SYNJ1	Synaptojanin 1	Protein Coding	1
12	IQGAP1	IQ Motif Containing GTPase Activating Protein 1	Protein Coding	1
13	DPM1	Dolichyl-Phosphate Mannosyltransferase Subunit 1, Catalytic	Protein Coding	1
14	EIF3H	Eukaryotic Translation Initiation Factor 3 Subunit H	Protein Coding	1
15	EIF3D	Eukaryotic Translation Initiation Factor 3 Subunit D	Protein Coding	1
16	PRKRA	Protein Activator Of Interferon Induced Protein Kinase EIF2AK2	Protein Coding	1
17	CGNL1	Cingulin Like 1	Protein Coding	1
18	TUBA1C	Tubulin Alpha 1c	Protein Coding	1
19	SLC25A11	Solute Carrier Family 25 Member 11	Protein Coding	1
20	KATNAL2	Katanin Catalytic Subunit A1 Like 2	Protein Coding	1
21	SH3BGRL3	SH3 Domain Binding Glutamate Rich Protein Like 3	Protein Coding	1
22	CAPZB	Capping Actin Protein Of Muscle Z-Line Subunit Beta	Protein Coding	1
23	TXNDC5	Thioredoxin Domain Containing 5	Protein Coding	1
24	CALU	Calumenin	Protein Coding	1
25	CALR	Calreticulin	Protein Coding	1
26	CACNA2D1	Calcium Voltage-Gated Channel Auxiliary Subunit Alpha2delta 1	Protein Coding	1
27	YWHAE	Tyrosine 3-Monooxygenase/Tryptophan 5-Monooxygenase Activation Protein Epsilon	Protein Coding	1
28	TPM3	Tropomyosin 3	Protein Coding	1
29	TMSB4X	Thymosin Beta 4 X-Linked	Protein Coding	1
30	TMOD1	Tropomodulin 1	Protein Coding	1
31	ACTG1	Actin Gamma 1	Protein Coding	1
32	TKT	Transketolase	Protein Coding	1
33	TFAM	Transcription Factor A, Mitochondrial	Protein Coding	1
34	PRDX2	Peroxiredoxin 2	Protein Coding	1
35	ELOC	Elongin C	Protein Coding	1
36	TBCA	Tubulin Folding Cofactor A	Protein Coding	1
37	BSG	Basigin (Ok Blood Group)	Protein Coding	1
38	SSR4	Signal Sequence Receptor Subunit 4	Protein Coding	1
39	SSR3	Signal Sequence Receptor Subunit 3	Protein Coding	1
40	SRP54	Signal Recognition Particle 54	Protein Coding	1
41	FSCN1	Fascin Actin-Bundling Protein 1	Protein Coding	1
42	SET	SET Nuclear Proto-Oncogene	Protein Coding	1
43	SARS1	Seryl-TRNA Synthetase 1	Protein Coding	1
44	RPLP2	Ribosomal Protein Lateral Stalk Subunit P2	Protein Coding	1
45	RPL27	Ribosomal Protein L27	Protein Coding	1
46	RPL26	Ribosomal Protein L26	Protein Coding	1
47	RPL5	Ribosomal Protein L5	Protein Coding	1
48	RCN1	Reticulocalbin 1	Protein Coding	1
49	PTPN14	Protein Tyrosine Phosphatase Non-Receptor Type 14	Protein Coding	1
50	PTMA	Prothymosin Alpha	Protein Coding	1
51	PSMD11	Proteasome 26S Subunit, Non-ATPase 11	Protein Coding	1
52	HTRA1	HtrA Serine Peptidase 1	Protein Coding	1
53	LRRC59	Leucine Rich Repeat Containing 59	Protein Coding	1
54	PPP2CA	Protein Phosphatase 2 Catalytic Subunit Alpha	Protein Coding	1
55	ATP6V1E1	ATPase H+ Transporting V1 Subunit E1	Protein Coding	1
56	PGK1	Phosphoglycerate Kinase 1	Protein Coding	1
57	PGD	Phosphogluconate Dehydrogenase	Protein Coding	1
58	PFN1	Profilin 1	Protein Coding	1
59	INPP5K	Inositol Polyphosphate-5-Phosphatase K	Protein Coding	1
60	ARMCX1	Armadillo Repeat Containing X-Linked 1	Protein Coding	1
61	P4HB	Prolyl 4-Hydroxylase Subunit Beta	Protein Coding	1
62	OCRL	OCRL Inositol Polyphosphate-5-Phosphatase	Protein Coding	1
63	RPL10A	Ribosomal Protein L10a	Protein Coding	1
64	NCL	Nucleolin	Protein Coding	1
65	MYO6	Myosin VI	Protein Coding	1
66	MYO1C	Myosin IC	Protein Coding	1
67	MYH11	Myosin Heavy Chain 11	Protein Coding	1
68	LMAN1	Lectin, Mannose Binding 1	Protein Coding	1
69	LDHA	Lactate Dehydrogenase A	Protein Coding	1
70	CCN1	Cellular Communication Network Factor 1	Protein Coding	1
71	TUBB8	Tubulin Beta 8 Class VIII	Protein Coding	1
72	IDH2	Isocitrate Dehydrogenase (NADP(+)) 2	Protein Coding	1
73	HSP90AA1	Heat Shock Protein 90 Alpha Family Class A Member 1	Protein Coding	1
74	DNAJA1	DnaJ Heat Shock Protein Family (Hsp40) Member A1	Protein Coding	1
75	HMGB1	High Mobility Group Box 1	Protein Coding	1
76	HBD	Hemoglobin Subunit Delta	Protein Coding	1
77	ANXA1	Annexin A1	Protein Coding	1
78	GLUD1	Glutamate Dehydrogenase 1	Protein Coding	1
79	SND1	Staphylococcal Nuclease And Tudor Domain Containing 1	Protein Coding	1
80	PABPC1	Poly(A) Binding Protein Cytoplasmic 1	Protein Coding	1
81	GIGYF2	GRB10 Interacting GYF Protein 2	Protein Coding	1
82	GAPDH	Glyceraldehyde-3-Phosphate Dehydrogenase	Protein Coding	1
83	ACOT9	Acyl-CoA Thioesterase 9	Protein Coding	1
84	RPL13A	Ribosomal Protein L13a	Protein Coding	1
85	FN1	Fibronectin 1	Protein Coding	1
86	VPS39	VPS39 Subunit Of HOPS Complex	Protein Coding	1
87	KANK1	KN Motif And Ankyrin Repeat Domains 1	Protein Coding	1
88	COPG1	Coat Protein Complex I Subunit Gamma 1	Protein Coding	1
89	ALDOA	Aldolase, Fructose-Bisphosphate A	Protein Coding	1
90	EWSR1	EWS RNA Binding Protein 1	Protein Coding	1
91	ALB	Albumin	Protein Coding	1
92	EPB41	Erythrocyte Membrane Protein Band 4.1	Protein Coding	1
93	EIF4G1	Eukaryotic Translation Initiation Factor 4 Gamma 1	Protein Coding	1
94	DSC1	Desmocollin 1	Protein Coding	1
95	DECR1	2,4-Dienoyl-CoA Reductase 1	Protein Coding	1
96	FGD5	FYVE, RhoGEF And PH Domain Containing 5	Protein Coding	1
97	CSRP2	Cysteine And Glycine Rich Protein 2	Protein Coding	1
98	CSRP1	Cysteine And Glycine Rich Protein 1	Protein Coding	1
99	CNP	2'''',3''''-Cyclic Nucleotide 3'''' Phosphodiesterase	Protein Coding	1
100	TPP1	Tripeptidyl Peptidase 1	Protein Coding	1
101	CLIC1	Chloride Intracellular Channel 1	Protein Coding	1
102	AP2S1	Adaptor Related Protein Complex 2 Subunit Sigma 1	Protein Coding	1
103	ASCC3	Activating Signal Cointegrator 1 Complex Subunit 3	Protein Coding	1
104	STIP1	Stress Induced Phosphoprotein 1	Protein Coding	1
105	CCT7	Chaperonin Containing TCP1 Subunit 7	Protein Coding	1
106	HYOU1	Hypoxia Up-Regulated 1	Protein Coding	1
107	ABCF2	ATP Binding Cassette Subfamily F Member 2	Protein Coding	1
108	FARSB	Phenylalanyl-TRNA Synthetase Subunit Beta	Protein Coding	1
109	EIF4G2	Eukaryotic Translation Initiation Factor 4 Gamma 2	Protein Coding	1
110	DHX36	DEAH-Box Helicase 36	Protein Coding	1
111	AP2A1	Adaptor Related Protein Complex 2 Subunit Alpha 1	Protein Coding	1
112	UBAP2L	Ubiquitin Associated Protein 2 Like	Protein Coding	1
113	PDE4DIP	Phosphodiesterase 4D Interacting Protein	Protein Coding	1
114	RBM39	RNA Binding Motif Protein 39	Protein Coding	1
115	FXR2	FMR1 Autosomal Homolog 2	Protein Coding	1
116	LRRFIP2	LRR Binding FLII Interacting Protein 2	Protein Coding	1
117	ATP6V0D1	ATPase H+ Transporting V0 Subunit D1	Protein Coding	1
118	FMNL3	Formin Like 3	Protein Coding	1
119	USP10	Ubiquitin Specific Peptidase 10	Protein Coding	1
120	NAPA	NSF Attachment Protein Alpha	Protein Coding	1
121	EIF3F	Eukaryotic Translation Initiation Factor 3 Subunit F	Protein Coding	1
122	NUMB	NUMB Endocytic Adaptor Protein	Protein Coding	1
123	CRIP2	Cysteine Rich Protein 2	Protein Coding	1
124	CCDC124	Coiled-Coil Domain Containing 124	Protein Coding	1
125	DNAJB4	DnaJ Heat Shock Protein Family (Hsp40) Member B4	Protein Coding	1
126	PDIA6	Protein Disulfide Isomerase Family A Member 6	Protein Coding	1
127	ARPC5L	Actin Related Protein 2/3 Complex Subunit 5 Like	Protein Coding	1
128	TFCP2	Transcription Factor CP2	Protein Coding	1
129	SRPK1	SRSF Protein Kinase 1	Protein Coding	1
130	RPS11	Ribosomal Protein S11	Protein Coding	1
131	RPL18A	Ribosomal Protein L18a	Protein Coding	1
132	RPL7	Ribosomal Protein L7	Protein Coding	1
133	PBXIP1	PBX Homeobox Interacting Protein 1	Protein Coding	1
134	PSMD4	Proteasome 26S Subunit Ubiquitin Receptor, Non-ATPase 4	Protein Coding	1
135	SPIRE1	Spire Type Actin Nucleation Factor 1	Protein Coding	1
136	ZC3H15	Zinc Finger CCCH-Type Containing 15	Protein Coding	1
137	LUC7L	LUC7 Like	Protein Coding	1
138	RPL39P5	Ribosomal Protein L39 Pseudogene 5	Pseudogene	1
139	PPP1CA	Protein Phosphatase 1 Catalytic Subunit Alpha	Protein Coding	1
140	PPM1G	Protein Phosphatase, Mg2+/Mn2+ Dependent 1G	Protein Coding	1
141	DHX29	DExH-Box Helicase 29	Protein Coding	1
142	NAP1L1	Nucleosome Assembly Protein 1 Like 1	Protein Coding	1
143	MOV10	Mov10 RNA Helicase	Protein Coding	1
144	HSP90AB2P	Heat Shock Protein 90 Alpha Family Class B Member 2, Pseudogene	Pseudogene	1
145	SHROOM2	Shroom Family Member 2	Protein Coding	1
146	TAOK2	TAO Kinase 2	Protein Coding	1
147	TMOD3	Tropomodulin 3	Protein Coding	1
148	GRSF1	G-Rich RNA Sequence Binding Factor 1	Protein Coding	1
149	FHOD1	Formin Homology 2 Domain Containing 1	Protein Coding	1
150	PRRC2C	Proline Rich Coiled-Coil 2C	Protein Coding	1
151	FAM120A	Family With Sequence Similarity 120 Member A	Protein Coding	1
152	FLII	FLII Actin Remodeling Protein	Protein Coding	1
153	EPRS1	Glutamyl-Prolyl-TRNA Synthetase 1	Protein Coding	1

Disorders associated with VEGFA-VEGFR2 signaling SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Diamond-blackfan anemia	Enrichment	RPL26, RPL27, RPL5	2.12
2	Cole-carpenter syndrome 1	Enrichment	P4HB	1.95
3	Phosphoglycerate kinase 1 deficiency	Enrichment	PGK1	1.95
4	Congenital disorder of glycosylation, type iy	Enrichment	SSR4	1.95
5	Hypocalciuric hypercalcemia, familial, type iii	Enrichment	AP2S1	1.95
6	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia	Enrichment	HMGB1	1.95
7	Rajab interstitial lung disease with brain calcifications 1	Enrichment	FARSB	1.95
8	Macular degeneration, age-related, 7	Enrichment	HTRA1	1.95
9	Deafness, autosomal dominant 22	Enrichment	MYO6	1.95
10	Parkinson disease 11, autosomal dominant	Enrichment	GIGYF2	1.95
11	Spinocerebellar ataxia, autosomal recessive 7	Enrichment	TPP1	1.95
12	Congenital myopathy 4b, autosomal recessive	Enrichment	TPM3	1.95
13	Parkinson disease 18, autosomal dominant	Enrichment	EIF4G1	1.95
14	Amyotrophic lateral sclerosis 18	Enrichment	PFN1	1.95
15	Short stature, developmental delay, and congenital heart defects	Enrichment	TKT	1.95
16	Myopia 25, autosomal dominant	Enrichment	P4HA2	1.95
17	Hyperthyroxinemia, familial dysalbuminemic	Enrichment	ALB	1.95
18	Elliptocytosis 1	Enrichment	EPB41	1.95
19	Developmental and epileptic encephalopathy 53	Enrichment	SYNJ1	1.95
20	Cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 2	Enrichment	HTRA1	1.95
21	Neurodevelopmental disorder with microcephaly, ataxia, and seizures	Enrichment	SARS1	1.95
22	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies	Enrichment	UBAP2L	1.95
23	Cardiomyopathy, dilated, 2j	Enrichment	FLII	1.95
24	Leukodystrophy, hypomyelinating, 20	Enrichment	CNP	1.95
25	Deafness, autosomal recessive 37	Enrichment	MYO6	1.95
26	Oocyte/zygote/embryo maturation arrest 24	Enrichment	TUBA1C	1.95
27	Lowe oculocerebrorenal syndrome	Enrichment	OCRL	1.95
28	Spinal muscular atrophy with congenital bone fractures 1	Enrichment	TRIP4	1.95
29	Bcard syndrome	Enrichment	PLOD3	1.95
30	Muscular dystrophy, congenital, davignon-chauveau type	Enrichment	TRIP4	1.95
31	Hyperinsulinemic hypoglycemia, familial, 6	Enrichment	GLUD1	1.95
32	Gemistocytic astrocytoma	Enrichment	IDH2	1.95
33	Protoplasmic astrocytoma	Enrichment	IDH2	1.95
34	Cerebral palsy, spastic quadriplegic, 2	Enrichment	KANK1	1.95
35	Diamond-blackfan anemia 11	Enrichment	RPL26	1.95
36	D-2-hydroxyglutaric aciduria 2	Enrichment	IDH2	1.95
37	Choanal atresia and lymphedema	Enrichment	PTPN14	1.95
38	Developmental and epileptic encephalopathy 110	Enrichment	CACNA2D1	1.95
39	Muscular dystrophy, congenital, with cataracts and impaired intellectual development	Enrichment	INPP5K	1.95
40	Mixed oligodendroglioma-astrocytoma	Enrichment	IDH2	1.95
41	Anaplastic oligoastrocytoma	Enrichment	IDH2	1.95
42	Chilton-okur-chung neurodevelopmental syndrome	Enrichment	CDC42BPB	1.95
43	Congenital analbuminemia	Enrichment	ALB	1.95
44	Cutis laxa, autosomal recessive, type iic	Enrichment	ATP6V1E1	1.95
45	Congenital myopathy 21 with early respiratory failure	Enrichment	DNAJB4	1.95
46	Leukodystrophy, hypomyelinating, 15	Enrichment	EPRS1	1.95
47	Pheochromocytoma/paraganglioma syndrome 6	Enrichment	SLC25A11	1.95
48	Analbuminemia	Enrichment	ALB	1.95
49	Intellectual developmental disorder, autosomal recessive 81	Enrichment	ASCC3	1.95
50	Fibrillary astrocytoma	Enrichment	IDH2	1.95
51	Acute myocardial infarction	Enrichment	IDH2	1.95
52	Brain calcification, rajab type	Enrichment	FARSB	1.95
53	Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome	Enrichment	MYO6	1.95
54	Cardiomyopathy, dilated, 2m	Enrichment	NEXN	1.95
55	Kuhnt-junius degeneration	Enrichment	HTRA1	1.95
56	Asymetric thumb-handgrip weakness-distal myopathy	Enrichment	DNAJB4	1.95
57	Immunodeficiency 128	Enrichment	COPG1	1.95
58	Autosomal dominant nonsyndromic hearing loss 22	Enrichment	MYO6	1.95
59	Liver cirrhosis	Enrichment	FARSB	1.95
60	Htra1 disorder	Enrichment	HTRA1	1.95
61	Htra1-related autosomal dominant cerebral small vessel disease	Enrichment	HTRA1	1.95
62	Lymphedema-posterior choanal atresia syndrome	Enrichment	PTPN14	1.95
63	Male infertility due to obstructive azoospermia	Enrichment	PGK1	1.95
64	Congenital generalized hypercontractile muscle stiffness syndrome	Enrichment	TPM3	1.95
65	Distal 17p13.3 microdeletion syndrome	Enrichment	YWHAE	1.95
66	Htra1-related cerebral small vessel disease	Enrichment	HTRA1	1.95
67	Rare autosomal dominant non-syndromic sensorineural deafness type dfna	Enrichment	ACTG1, MYO1C, MYO6	1.68
68	Aortic aneurysm, familial thoracic 4	Enrichment	MYH11	1.65
69	Spondyloepimetaphyseal dysplasia, strudwick type	Enrichment	FN1	1.65
70	Fanconi-bickel syndrome	Enrichment	LDHA	1.65
71	Spondylometaphyseal dysplasia, corner fracture type	Enrichment	FN1	1.65
72	Ceroid lipofuscinosis, neuronal, 2	Enrichment	TPP1	1.65
73	Immunodeficiency 59 and hypoglycemia	Enrichment	HYOU1	1.65
74	Dent disease 2	Enrichment	OCRL	1.65
75	Histiocytoma, angiomatoid fibrous	Enrichment	EWSR1	1.65
76	Diamond-blackfan anemia 6	Enrichment	RPL5	1.65
77	Deafness, autosomal dominant 20	Enrichment	ACTG1	1.65
78	Baraitser-winter syndrome 2	Enrichment	ACTG1	1.65
79	Vitreoretinal degeneration, snowflake type	Enrichment	GIGYF2	1.65
80	Parkinson disease 20, early-onset	Enrichment	SYNJ1	1.65
81	Cardiomyopathy, dilated, 1cc	Enrichment	NEXN	1.65
82	Leber congenital amaurosis 16	Enrichment	GIGYF2	1.65
83	Dystonia 16	Enrichment	PRKRA	1.65
84	Ceroid lipofuscinosis, neuronal, 3	Enrichment	TPP1	1.65
85	Intellectual developmental disorder, autosomal recessive 67	Enrichment	EIF3F	1.65
86	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2	Enrichment	MYH11	1.65
87	Neutropenia, severe congenital, 8, autosomal dominant	Enrichment	SRP54	1.65
88	Microcephaly 21, primary, autosomal recessive	Enrichment	GAPDH	1.65
89	Glycogen storage disease xii	Enrichment	ALDOA	1.65
90	Oligodendroglioma	Enrichment	IDH2	1.65
91	Cardiomyopathy, familial hypertrophic, 20	Enrichment	NEXN	1.65
92	Angiocentric glioma	Enrichment	QKI	1.65
93	Hemoglobin lepore-beta-thalassemia syndrome	Enrichment	HBD	1.65
94	Interstitial lung and liver disease	Enrichment	FARSB	1.65
95	Visceral myopathy 2	Enrichment	MYH11	1.65
96	Baraitser-winter cerebrofrontofacial syndrome	Enrichment	ACTG1	1.65
97	Diamond-blackfan anemia 16	Enrichment	RPL27	1.65
98	Anaplastic oligodendroglioma	Enrichment	IDH2	1.65
99	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2	Enrichment	HTRA1	1.65
100	Mitochondrial dna depletion syndrome 15	Enrichment	TFAM	1.65
101	Houge-janssens syndrome 3	Enrichment	PPP2CA	1.65
102	Intellectual developmental disorder, autosomal dominant 58	Enrichment	SET	1.65
103	Prenatal-onset spinal muscular atrophy with congenital bone fractures	Enrichment	TRIP4	1.65
104	Combined deficiency of factor v and factor viii	Enrichment	LMAN1	1.65
105	D-2-hydroxyglutaric aciduria	Enrichment	IDH2	1.65
106	Sickle cell s-lepore disease	Enrichment	HBD	1.65
107	Malignant peripheral nerve sheath tumor with perineurial differentiation	Enrichment	HTRA1	1.65
108	Desmoplastic small round cell tumor	Enrichment	EWSR1	1.65
109	Malignant triton tumor	Enrichment	HTRA1	1.65
110	Centronuclear myopathy	Enrichment	TPM3, TRIP4	1.64
111	Parkinson disease, late-onset	Enrichment	EIF4G1, GIGYF2	1.53
112	Myopia 2, autosomal dominant	Enrichment	CNP	1.48
113	Thrombocythemia 1	Enrichment	CALR	1.48
114	Factor v and factor viii, combined deficiency of, 1	Enrichment	LMAN1	1.48
115	Glomerulopathy with fibronectin deposits 2	Enrichment	FN1	1.48
116	Miller-dieker lissencephaly syndrome	Enrichment	YWHAE	1.48
117	Chromosome 17p13.3, centromeric, duplication syndrome	Enrichment	YWHAE	1.48
118	Oocyte/zygote/embryo maturation arrest 2	Enrichment	TUBB8	1.48
119	Dent disease	Enrichment	OCRL	1.48
120	Autosomal recessive cutis laxa type ii classic type	Enrichment	ATP6V1E1	1.48
121	Anaplastic astrocytoma	Enrichment	IDH2	1.48
122	Atypical juvenile parkinsonism	Enrichment	SYNJ1	1.48
123	Cole-carpenter syndrome	Enrichment	P4HB	1.48
124	Cap myopathy	Enrichment	TPM3	1.48
125	Melanoma of soft tissue	Enrichment	EWSR1	1.48
126	Tricuspid valve insufficiency	Enrichment	MYH11	1.48
127	Delta beta-thalassemia	Enrichment	HBD	1.48
128	Ehlers-danlos syndrome, arthrochalasia type, 1	Enrichment	ALB	1.35
129	Megacystis-microcolon-intestinal hypoperistalsis syndrome 1	Enrichment	MYH11	1.35
130	Temporal arteritis	Enrichment	P4HA2	1.35
131	Budd-chiari syndrome	Enrichment	CALR	1.35
132	Imerslund-grasbeck syndrome 2	Enrichment	CDC42BPB	1.35
133	Hereditary elliptocytosis	Enrichment	EPB41	1.35
134	Spastic quadriplegic cerebral palsy	Enrichment	KANK1	1.35
135	Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)	Enrichment	MYH11	1.35
136	Mitral valve insufficiency	Enrichment	MYH11	1.35
137	Intermediate nemaline myopathy	Enrichment	TPM3	1.35
138	Enchondromatosis, multiple, ollier type	Enrichment	IDH2	1.26
139	Visceral myopathy 1	Enrichment	MYH11	1.26
140	Smith-magenis syndrome	Enrichment	FLII	1.26
141	Chondrosarcoma, extraskeletal myxoid	Enrichment	EWSR1	1.26
142	Ciliary dyskinesia, primary, 40	Enrichment	SRP54	1.26
143	Cardiac arrest	Enrichment	CACNA2D1	1.26
144	Hemangioma	Enrichment	RPL5	1.26
145	Female infertility due to oocyte meiotic arrest	Enrichment	TUBB8	1.26
146	Congenital short qt syndrome	Enrichment	CACNA2D1	1.26
147	Coloboma of choroid and retina	Enrichment	ACTG1	1.26
148	Endometrial stromal sarcoma	Enrichment	YWHAE	1.26
149	Non-syndromic genetic deafness	Enrichment	ACTG1, MYO6	1.21
150	Hyperaldosteronism, familial, type i	Enrichment	HBD	1.18
151	Angelman syndrome	Enrichment	TPP1	1.18
152	Osteogenesis imperfecta, type i	Enrichment	P4HB	1.18
153	Hyperinsulinemic hypoglycemia, familial, 1	Enrichment	GLUD1	1.18
154	Shwachman-diamond syndrome 1	Enrichment	SRP54	1.18
155	Epidermolysis bullosa, junctional 5b, with pyloric atresia	Enrichment	MYO6	1.18
156	Developmental and epileptic encephalopathy 36	Enrichment	DPM1	1.18
157	Inflammatory myofibroblastic tumor	Enrichment	TPM3	1.18
158	Intestinal pseudo-obstruction	Enrichment	MYH11	1.18
159	Megaloblastic anemia	Enrichment	CDC42BPB	1.18
160	Kidney clear cell sarcoma	Enrichment	YWHAE	1.18
161	Nonsyndromic genetic hyperinsulinism	Enrichment	GLUD1	1.18
162	Meniere disease	Enrichment	SHROOM2	1.12
163	Myelofibrosis	Enrichment	CALR	1.12
164	Imerslund-grasbeck syndrome 1	Enrichment	CDC42BPB	1.12
165	Brugada syndrome 1	Enrichment	CACNA2D1	1.12
166	Multiple enchondromatosis, maffucci type	Enrichment	IDH2	1.12
167	Essential thrombocythemia	Enrichment	CALR	1.12
168	Childhood-onset nemaline myopathy	Enrichment	TPM3	1.12
169	Nonsyndromic hearing loss	Enrichment	ACTG1, MYO6	1.09
170	Glioma susceptibility 1	Enrichment	IDH2	1.06
171	Ewing sarcoma	Enrichment	EWSR1	1.06
172	Neurofibromatosis, type i	Enrichment	EWSR1	1.01
173	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies	Enrichment	EIF3F	1.01
174	Familial thoracic aortic aneurysm and dissection	Enrichment	MYH11	1.01
175	Cat eye syndrome	Enrichment	ACTG1	0.97
176	Aplastic anemia	Enrichment	RPL5	0.97
177	Nemaline myopathy	Enrichment	TPM3	0.97
178	Atrial heart septal defect	Enrichment	RPL5	0.93
179	Interatrial communication	Enrichment	RPL5	0.93
180	Early-onset parkinson's disease	Enrichment	SYNJ1	0.90
181	Cutis laxa	Enrichment	ATP6V1E1	0.90
182	Undetermined early-onset epileptic encephalopathy	Enrichment	CACNA2D1, SYNJ1	0.88
183	Pulmonary hypertension, primary, 1	Enrichment	RPL5	0.86
184	Aortic aneurysm, familial thoracic 1	Enrichment	MYH11	0.83
185	Heart disease	Enrichment	NEXN	0.83
186	Congenital myopathy 4a, autosomal dominant	Enrichment	TPM3	0.81
187	Myopia	Enrichment	MYH11	0.81
188	Neuronal ceroid lipofuscinosis	Enrichment	TPP1	0.81
189	Cardiomyopathy, dilated, 1e	Enrichment	NEXN	0.76
190	Congenital disorder of glycosylation, type in	Enrichment	SSR3	0.76
191	Arteriovenous malformations of the brain	Enrichment	SARS1	0.71
192	Congenital myopathy	Enrichment	ASCC3	0.71
193	Lissencephaly	Enrichment	ACTG1	0.67
194	Hereditary paraganglioma-pheochromocytoma syndromes	Enrichment	SLC25A11	0.67
195	Myocardial infarction	Enrichment	CCT7	0.66
196	Rare genetic deafness	Enrichment	ACTG1, MYO6	0.65
197	Dilated cardiomyopathy	Enrichment	FLII, NEXN	0.64
198	Diamond-blackfan anemia 1	Enrichment	RPL5	0.64
199	Precursor t-cell acute lymphoblastic leukemia	Enrichment	SET	0.64
200	Ear malformation	Enrichment	MYO6	0.62
201	Developmental and epileptic encephalopathy 1	Enrichment	SYNJ1	0.61
202	Brugada syndrome	Enrichment	CACNA2D1	0.59
203	Rasopathy	Enrichment	ATP6V1E1	0.59
204	Primary autosomal recessive microcephaly	Enrichment	SARS1	0.52
205	Cakut	Enrichment	ACTG1	0.49
206	Left ventricular noncompaction	Enrichment	NEXN	0.48
207	Leukemia, acute myeloid	Enrichment	IDH2	0.44
208	Myopathy	Enrichment	TPM3	0.44
209	Nephrotic syndrome	Enrichment	FN1	0.41
210	West syndrome	Enrichment	SYNJ1	0.41
211	Familial thoracic aortic aneurysm and aortic dissection	Enrichment	MYH11	0.41
212	Autosomal dominant non-syndromic intellectual disability	Enrichment	SET	0.36
213	Familial isolated dilated cardiomyopathy	Enrichment	NEXN	0.34
214	Frontotemporal dementia and/or amyotrophic lateral sclerosis 7	Enrichment	PFN1	0.32
215	Autosomal recessive non-syndromic intellectual disability	Enrichment	SARS1	0.32
216	Schizophrenia	Enrichment	KATNAL2	0.31
217	Breast cancer	Enrichment	CACNA2D1	0.24
218	Rare autosomal recessive non-syndromic sensorineural deafness type dfnb	Enrichment	MYO6	0.20
219	Leber plus disease	Enrichment	GIGYF2	0.18
220	Congenital nervous system abnormality	Enrichment	TPP1	0.15
221	Nervous system disease	Enrichment	TPP1	0.15
222	Autism spectrum disorder	Enrichment	CDC42BPB	0.15
223	Microcephaly	Enrichment	ACTG1	0.12
224	Complex neurodevelopmental disorder	Enrichment	PPP2CA	0.12
225	Retinitis pigmentosa	Enrichment	GIGYF2	0.04

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

VEGFA-VEGFR2 signaling

Pathway Network for VEGFA-VEGFR2 signaling

Member Pathways for VEGFA-VEGFR2 signaling

Pathways in the VEGFA-VEGFR2 signaling SuperPath

Associated Genes for VEGFA-VEGFR2 signaling

Associated Disorders for VEGFA-VEGFR2 signaling

Disorders associated with VEGFA-VEGFR2 signaling SuperPath

STRING Interaction Network for VEGFA-VEGFR2 signaling

Sources for VEGFA-VEGFR2 signaling