Guidance Cues and Growth Cone Motility

No Pathway Network information available for Guidance Cues and Growth Cone Motility

Pathways in the Guidance Cues and Growth Cone Motility SuperPath

#	Name	Source	Genes
1	Guidance Cues and Growth Cone Motility	QIAGEN	ABL1 ABL2 ACTR2 ACTR3 ARHGEF1 ARHGEF10 ARHGEF11 ARHGEF12 ARHGEF15 ARHGEF16 ARHGEF2 ARHGEF3 ARHGEF4 ARHGEF5 ARHGEF6 ARHGEF7 ARHGEF9 BDNF CABLES1 CDC42 CDK5 CFL1 CFL2 CLEC18C CRMP1 DAB1 DCC DIRAS3 DPYSL5 DSCAM EFNA1 EFNA2 EFNA3 EFNA4 EFNA5 EPHA1 EPHA2 EPHA3 EPHA4 EPHA5 EPHA7 EPHA8 FES FYN GDAP1 GSN LIMK1 LIMK2 LRP8 MAG MAPK8IP2 MCF2L MYL1 MYL11 MYL2 MYL3 MYL4 MYL5 MYL6 MYL7 MYL9 NCK1 NCK2 NET1 NGEF NGF NGFR NRP1 NTN1 NTRK1 NTRK2 NTRK3 PAK1 PAK2 PAK3 PAK4 PAK5 PAK6 PIK3R1 PIK3R2 PIK3R3 PIK3R4 PIK3R5 PLCG1 PLCG2 PLXNB1 RAC1 RAC2 RAC3 RASA1 RELN RHOA RHOB RHOC RHOD RHOG RHOH RND2 RND3 ROBO1 ROCK1 ROCK2 RTN4R SEMA3A SEMA4D SLIT1 SLIT2 SLIT3 SRGAP1 SRGAP2 SRGAP3 UNC5A UNC5B UNC5C UNC5D VLDLR WASL (see all 117) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	ABL1	ABL Proto-Oncogene 1, Non-Receptor Tyrosine Kinase	Protein Coding	1
2	ABL2	ABL Proto-Oncogene 2, Non-Receptor Tyrosine Kinase	Protein Coding	1
3	ACTR2	Actin Related Protein 2	Protein Coding	1
4	ACTR3	Actin Related Protein 3	Protein Coding	1
5	RHOA	Ras Homolog Family Member A	Protein Coding	1
6	RHOB	Ras Homolog Family Member B	Protein Coding	1
7	RHOC	Ras Homolog Family Member C	Protein Coding	1
8	RHOD	Ras Homolog Family Member D	Protein Coding	1
9	RND3	Rho Family GTPase 3	Protein Coding	1
10	RHOG	Ras Homolog Family Member G	Protein Coding	1
11	ARHGEF1	Rho Guanine Nucleotide Exchange Factor 1	Protein Coding	1
12	ARHGEF10	Rho Guanine Nucleotide Exchange Factor 10	Protein Coding	1
13	ARHGEF11	Rho Guanine Nucleotide Exchange Factor 11	Protein Coding	1
14	ARHGEF12	Rho Guanine Nucleotide Exchange Factor 12	Protein Coding	1
15	ARHGEF15	Rho Guanine Nucleotide Exchange Factor 15	Protein Coding	1
16	ARHGEF16	Rho Guanine Nucleotide Exchange Factor 16	Protein Coding	1
17	ARHGEF2	Rho/Rac Guanine Nucleotide Exchange Factor 2	Protein Coding	1
18	ARHGEF3	Rho Guanine Nucleotide Exchange Factor 3	Protein Coding	1
19	ARHGEF4	Rho Guanine Nucleotide Exchange Factor 4	Protein Coding	1
20	ARHGEF5	Rho Guanine Nucleotide Exchange Factor 5	Protein Coding	1
21	ARHGEF6	Rac/Cdc42 Guanine Nucleotide Exchange Factor 6	Protein Coding	1
22	ARHGEF7	Rho Guanine Nucleotide Exchange Factor 7	Protein Coding	1
23	ARHGEF9	Cdc42 Guanine Nucleotide Exchange Factor 9	Protein Coding	1
24	RHOH	Ras Homolog Family Member H	Protein Coding	1
25	DIRAS3	DIRAS Family GTPase 3	Protein Coding	1
26	RND2	Rho Family GTPase 2	Protein Coding	1
27	BDNF	Brain Derived Neurotrophic Factor	Protein Coding	1
28	CABLES1	Cdk5 And Abl Enzyme Substrate 1	Protein Coding	1
29	CDC42	Cell Division Cycle 42	Protein Coding	1
30	CDK5	Cyclin Dependent Kinase 5	Protein Coding	1
31	CFL1	Cofilin 1	Protein Coding	1
32	CFL2	Cofilin 2	Protein Coding	1
33	CRMP1	Collapsin Response Mediator Protein 1	Protein Coding	1
34	DAB1	DAB Adaptor Protein 1	Protein Coding	1
35	DCC	DCC Netrin 1 Receptor	Protein Coding	1
36	DPYSL5	Dihydropyrimidinase Like 5	Protein Coding	1
37	DSCAM	DS Cell Adhesion Molecule	Protein Coding	1
38	EFNA1	Ephrin A1	Protein Coding	1
39	EFNA2	Ephrin A2	Protein Coding	1
40	EFNA3	Ephrin A3	Protein Coding	1
41	EFNA4	Ephrin A4	Protein Coding	1
42	EFNA5	Ephrin A5	Protein Coding	1
43	EPHA1	EPH Receptor A1	Protein Coding	1
44	EPHA2	EPH Receptor A2	Protein Coding	1
45	EPHA3	EPH Receptor A3	Protein Coding	1
46	EPHA4	EPH Receptor A4	Protein Coding	1
47	EPHA5	EPH Receptor A5	Protein Coding	1
48	EPHA7	EPH Receptor A7	Protein Coding	1
49	EPHA8	EPH Receptor A8	Protein Coding	1
50	FES	FES Proto-Oncogene, Tyrosine Kinase	Protein Coding	1
51	FYN	FYN Proto-Oncogene, Src Family Tyrosine Kinase	Protein Coding	1
52	GDAP1	Ganglioside Induced Differentiation Associated Protein 1	Protein Coding	1
53	GSN	Gelsolin	Protein Coding	1
54	MYL11	Myosin Light Chain 11	Protein Coding	1
55	LIMK1	LIM Domain Kinase 1	Protein Coding	1
56	LIMK2	LIM Domain Kinase 2	Protein Coding	1
57	LRP8	LDL Receptor Related Protein 8	Protein Coding	1
58	MAG	Myelin Associated Glycoprotein	Protein Coding	1
59	MAPK8IP2	Mitogen-Activated Protein Kinase 8 Interacting Protein 2	Protein Coding	1
60	MCF2L	MCF.2 Cell Line Derived Transforming Sequence Like	Protein Coding	1
61	CLEC18C	C-Type Lectin Domain Family 18 Member C	Protein Coding	1
62	MYL1	Myosin Light Chain 1	Protein Coding	1
63	MYL2	Myosin Light Chain 2	Protein Coding	1
64	MYL3	Myosin Light Chain 3	Protein Coding	1
65	MYL4	Myosin Light Chain 4	Protein Coding	1
66	MYL5	Myosin Light Chain 5	Protein Coding	1
67	MYL6	Myosin Light Chain 6	Protein Coding	1
68	MYL7	Myosin Light Chain 7	Protein Coding	1
69	MYL9	Myosin Light Chain 9	Protein Coding	1
70	NCK1	NCK Adaptor Protein 1	Protein Coding	1
71	NCK2	NCK Adaptor Protein 2	Protein Coding	1
72	NET1	Neuroepithelial Cell Transforming 1	Protein Coding	1
73	NGEF	Neuronal Guanine Nucleotide Exchange Factor	Protein Coding	1
74	NGF	Nerve Growth Factor	Protein Coding	1
75	NGFR	Nerve Growth Factor Receptor	Protein Coding	1
76	NRP1	Neuropilin 1	Protein Coding	1
77	NTN1	Netrin 1	Protein Coding	1
78	NTRK1	Neurotrophic Receptor Tyrosine Kinase 1	Protein Coding	1
79	NTRK2	Neurotrophic Receptor Tyrosine Kinase 2	Protein Coding	1
80	NTRK3	Neurotrophic Receptor Tyrosine Kinase 3	Protein Coding	1
81	PIK3R5	Phosphoinositide-3-Kinase Regulatory Subunit 5	Protein Coding	1
82	PAK1	P21 (RAC1) Activated Kinase 1	Protein Coding	1
83	PAK2	P21 (RAC1) Activated Kinase 2	Protein Coding	1
84	PAK3	P21 (RAC1) Activated Kinase 3	Protein Coding	1
85	PAK4	P21 (RAC1) Activated Kinase 4	Protein Coding	1
86	PAK6	P21 (RAC1) Activated Kinase 6	Protein Coding	1
87	PAK5	P21 (RAC1) Activated Kinase 5	Protein Coding	1
88	PIK3R1	Phosphoinositide-3-Kinase Regulatory Subunit 1	Protein Coding	1
89	PIK3R2	Phosphoinositide-3-Kinase Regulatory Subunit 2	Protein Coding	1
90	PIK3R3	Phosphoinositide-3-Kinase Regulatory Subunit 3	Protein Coding	1
91	PIK3R4	Phosphoinositide-3-Kinase Regulatory Subunit 4	Protein Coding	1
92	PLCG1	Phospholipase C Gamma 1	Protein Coding	1
93	PLCG2	Phospholipase C Gamma 2	Protein Coding	1
94	PLXNB1	Plexin B1	Protein Coding	1
95	RAC1	Rac Family Small GTPase 1	Protein Coding	1
96	RAC2	Rac Family Small GTPase 2	Protein Coding	1
97	RAC3	Rac Family Small GTPase 3	Protein Coding	1
98	RASA1	RAS P21 Protein Activator 1	Protein Coding	1
99	RELN	Reelin	Protein Coding	1
100	ROBO1	Roundabout Guidance Receptor 1	Protein Coding	1
101	ROCK1	Rho Associated Coiled-Coil Containing Protein Kinase 1	Protein Coding	1
102	ROCK2	Rho Associated Coiled-Coil Containing Protein Kinase 2	Protein Coding	1
103	RTN4R	Reticulon 4 Receptor	Protein Coding	1
104	SEMA3A	Semaphorin 3A	Protein Coding	1
105	SEMA4D	Semaphorin 4D	Protein Coding	1
106	SLIT1	Slit Guidance Ligand 1	Protein Coding	1
107	SLIT2	Slit Guidance Ligand 2	Protein Coding	1
108	SLIT3	Slit Guidance Ligand 3	Protein Coding	1
109	SRGAP1	SLIT-ROBO Rho GTPase Activating Protein 1	Protein Coding	1
110	SRGAP2	SLIT-ROBO Rho GTPase Activating Protein 2	Protein Coding	1
111	SRGAP3	SLIT-ROBO Rho GTPase Activating Protein 3	Protein Coding	1
112	UNC5A	Unc-5 Netrin Receptor A	Protein Coding	1
113	UNC5B	Unc-5 Netrin Receptor B	Protein Coding	1
114	UNC5C	Unc-5 Netrin Receptor C	Protein Coding	1
115	UNC5D	Unc-5 Netrin Receptor D	Protein Coding	1
116	VLDLR	Very Low Density Lipoprotein Receptor	Protein Coding	1
117	WASL	WASP Like Actin Nucleation Promoting Factor	Protein Coding	1

Disorders associated with Guidance Cues and Growth Cone Motility SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Mirror movements 1	Enrichment	DCC, NTN1	3.36
2	Neuropathy, hereditary sensory and autonomic, type v	Enrichment	NGF, NTRK1	2.82
3	Pilomyxoid astrocytoma	Enrichment	NTRK2, SRGAP3	2.82
4	Cakut	Enrichment	ROBO1, SLIT2, SRGAP1	2.51
5	Heart disease	Enrichment	ABL1, MYL2	2.20
6	Arthritis, sacroiliac	Enrichment	RELN	2.06
7	Cystic angiomatosis of bone, diffuse	Enrichment	RASA1	2.06
8	Nystagmus 8, congenital, autosomal recessive	Enrichment	ROBO1	2.06
9	Intellectual developmental disorder, x-linked 30	Enrichment	PAK3	2.06
10	Developmental and epileptic encephalopathy 8	Enrichment	ARHGEF9	2.06
11	Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis	Enrichment	RAC2	2.06
12	Cardiomyopathy, familial hypertrophic, 8	Enrichment	MYL3	2.06
13	Amyloidosis, finnish type	Enrichment	GSN	2.06
14	Ataxia-oculomotor apraxia 3	Enrichment	PIK3R5	2.06
15	Lissencephaly 7 with cerebellar hypoplasia	Enrichment	CDK5	2.06
16	Immunodeficiency 62	Enrichment	ARHGEF1	2.06
17	Neurodevelopmental disorder with midbrain and hindbrain malformations	Enrichment	ARHGEF2	2.06
18	Developmental and epileptic encephalopathy 58	Enrichment	NTRK2	2.06
19	Knobloch syndrome 2	Enrichment	PAK2	2.06
20	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies	Enrichment	RAC3	2.06
21	Short syndrome	Enrichment	PIK3R1	2.06
22	Intellectual developmental disorder with macrocephaly, seizures, and speech delay	Enrichment	PAK1	2.06
23	Immune dysregulation, autoimmunity, and autoinflammation	Enrichment	PLCG1	2.06
24	Mirror movements 4	Enrichment	NTN1	2.06
25	Intellectual developmental disorder, x-linked 46	Enrichment	ARHGEF6	2.06
26	Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia	Enrichment	RAC2	2.06
27	Atrial fibrillation, familial, 18	Enrichment	MYL4	2.06
28	Nemaline myopathy 7	Enrichment	CFL2	2.06
29	Slowed nerve conduction velocity, autosomal dominant	Enrichment	ARHGEF10	2.06
30	Immunodeficiency 36 with lymphoproliferation	Enrichment	PIK3R1	2.06
31	Autoinflammation, antibody deficiency, and immune dysregulation	Enrichment	PLCG2	2.06
32	Hypogonadotropic hypogonadism 16 with or without anosmia	Enrichment	SEMA3A	2.06
33	Spinocerebellar ataxia 37	Enrichment	DAB1	2.06
34	Synovitis	Enrichment	RELN	2.06
35	Agammaglobulinemia 7, autosomal recessive	Enrichment	PIK3R1	2.06
36	Obesity, hyperphagia, and developmental delay	Enrichment	NTRK2	2.06
37	Brain small vessel disease 5 with osteoporosis	Enrichment	ARHGEF15	2.06
38	Familial cold autoinflammatory syndrome 3	Enrichment	PLCG2	2.06
39	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies	Enrichment	RHOA	2.06
40	Spastic paraplegia 75, autosomal recessive	Enrichment	MAG	2.06
41	Takenouchi-kosaki syndrome	Enrichment	CDC42	2.06
42	Gaze palsy, familial horizontal, with progressive scoliosis 2, with impaired intellectual development	Enrichment	DCC	2.06
43	Autosomal recessive congenital nystagmus	Enrichment	ROBO1	2.06
44	Congenital myopathy 14	Enrichment	MYL1	2.06
45	Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies	Enrichment	RHOA	2.06
46	Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia	Enrichment	RAC2	2.06
47	Pituitary hormone deficiency, combined or isolated, 8	Enrichment	ROBO1	2.06
48	Immunodeficiency 129	Enrichment	RHOH	2.06
49	Ritscher-schinzel syndrome 4	Enrichment	DPYSL5	2.06
50	Cerebellar hypoplasia	Enrichment	VLDLR	2.06
51	Neurooculorenal syndrome	Enrichment	ROBO1	2.06
52	T-cell immunodeficiency with epidermodysplasia verruciformis	Enrichment	RHOH	2.06
53	Gorham's disease	Enrichment	RASA1	2.06
54	Infantile lad-like disease due to rac2 deficiency	Enrichment	RAC2	2.06
55	Reticular dysgenesis-like severe combined immunodeficiency	Enrichment	RAC2	2.06
56	Nocarh syndrome	Enrichment	CDC42	2.06
57	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom	Enrichment	RAC1	2.06
58	Rac2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome	Enrichment	RAC2	2.06
59	Congenital nystagmus	Enrichment	ROBO1	2.06
60	Kallmann syndrome	Enrichment	DCC, SEMA3A	1.78
61	Insensitivity to pain, congenital, with anhidrosis	Enrichment	NTRK1	1.77
62	Charcot-marie-tooth disease, demyelinating, type 4a	Enrichment	GDAP1	1.77
63	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2	Enrichment	PIK3R5	1.77
64	Charcot-marie-tooth disease, axonal, with vocal cord paresis, autosomal recessive	Enrichment	GDAP1	1.77
65	Charcot-marie-tooth disease, recessive intermediate a	Enrichment	GDAP1	1.77
66	Pain sensitivity quantitative trait locus 1	Enrichment	NTRK1	1.77
67	Intellectual developmental disorder, autosomal dominant 48	Enrichment	RAC1	1.77
68	Congenital heart defects and skeletal malformations syndrome	Enrichment	ABL1	1.77
69	Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome	Enrichment	VLDLR	1.77
70	Cardiomyopathy, familial hypertrophic, 10	Enrichment	MYL2	1.77
71	Congenital mesoblastic nephroma	Enrichment	NTRK3	1.77
72	Charcot-marie-tooth disease, axonal, type 2h	Enrichment	GDAP1	1.77
73	Axonal neuropathy	Enrichment	GDAP1	1.77
74	Immune system disease	Enrichment	CDC42	1.77
75	Fibrosarcoma	Enrichment	NTRK3	1.77
76	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy	Enrichment	MYL2	1.77
77	Arthrogryposis, distal, type 1c	Enrichment	MYL11	1.77
78	Megacystis-microcolon-intestinal hypoperistalsis syndrome 4	Enrichment	MYL9	1.77
79	Horizontal gaze palsy with progressive scoliosis	Enrichment	DCC	1.77
80	Arthritis	Enrichment	RELN	1.77
81	Charcot-marie-tooth disease type 4a	Enrichment	GDAP1	1.77
82	Thyroid carcinoma, familial medullary	Enrichment	NTRK1	1.59
83	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi	Enrichment	PIK3R1	1.59
84	Charcot-marie-tooth disease, axonal, type 2k	Enrichment	GDAP1	1.59
85	Epilepsy, familial temporal lobe, 7	Enrichment	RELN	1.59
86	Immunodeficiency 14a with lymphoproliferation, autosomal dominant	Enrichment	PIK3R1	1.59
87	Wieacker-wolff syndrome	Enrichment	RASA1	1.59
88	Immunodeficiency 14	Enrichment	PIK3R1	1.59
89	Kyphosis	Enrichment	RELN	1.59
90	T-cell acute lymphoblastic leukemia	Enrichment	ABL1	1.59
91	Epilepsy with auditory features	Enrichment	RELN	1.59
92	Differentiated thyroid carcinoma	Enrichment	NTRK1, NTRK3	1.59
93	Peripheral nervous system disease	Enrichment	GDAP1, NGF	1.51
94	Neuropathy	Enrichment	GDAP1, NGF	1.51
95	Familial hypertrophic cardiomyopathy	Enrichment	MYL2, MYL3	1.49
96	Amyotrophy, monomelic	Enrichment	SLIT1	1.47
97	Megalencephaly-capillary malformation-polymicrogyria syndrome	Enrichment	PIK3R2	1.47
98	Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1	Enrichment	PIK3R2	1.47
99	Chronic myelogenous leukemia, bcr-abl1 positive	Enrichment	ABL1	1.47
100	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia	Enrichment	CDC42	1.47
101	Knobloch syndrome	Enrichment	PAK2	1.47
102	Glioma	Enrichment	NTRK3	1.47
103	Cataract 6, multiple types	Enrichment	EPHA2	1.37
104	Capillary malformations, congenital	Enrichment	RASA1	1.37
105	Knobloch syndrome 1	Enrichment	PAK2	1.37
106	Mosaic variegated aneuploidy syndrome 1	Enrichment	PAK6	1.37
107	Lissencephaly 2	Enrichment	RELN	1.37
108	Cholangitis, primary sclerosing	Enrichment	SEMA4D	1.37
109	Polyneuropathy	Enrichment	GDAP1	1.37
110	Aniridia	Enrichment	EPHA2	1.37
111	Sensory peripheral neuropathy	Enrichment	GDAP1	1.37
112	Charcot-marie-tooth disease	Enrichment	ARHGEF10, GDAP1	1.31
113	Klippel-trenaunay-weber syndrome	Enrichment	RASA1	1.30
114	Telangiectasia, hereditary hemorrhagic, type 1	Enrichment	RASA1	1.30
115	Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 1	Enrichment	VLDLR	1.30
116	Hemihyperplasia, isolated	Enrichment	RHOA	1.30
117	Wilms tumor, aniridia, genitourinary anomalies, and impaired intellectual development syndrome	Enrichment	BDNF	1.30
118	Ritscher-schinzel syndrome 1	Enrichment	DPYSL5	1.30
119	Hemangioma, capillary infantile	Enrichment	RASA1	1.30
120	Basal cell carcinoma 1	Enrichment	RASA1	1.30
121	Typical nemaline myopathy	Enrichment	CFL2	1.30
122	Hypertrophic cardiomyopathy	Enrichment	MYL2, MYL3	1.28
123	Esophageal cancer	Enrichment	DCC	1.23
124	Thyroid cancer, nonmedullary, 2	Enrichment	SRGAP1	1.23
125	Capillary malformation-arteriovenous malformation 1	Enrichment	RASA1	1.23
126	Leukemia, chronic myeloid	Enrichment	ABL1	1.23
127	Hereditary hemorrhagic telangiectasia	Enrichment	RASA1	1.23
128	Follicular thyroid carcinoma	Enrichment	SRGAP1	1.23
129	Overgrowth syndrome	Enrichment	PIK3R1	1.23
130	Familial isolated restrictive cardiomyopathy	Enrichment	MYL2	1.23
131	Moyamoya angiopathy	Enrichment	ABL1	1.23
132	B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)	Enrichment	ABL1	1.23
133	Mosaic variegated aneuploidy syndrome	Enrichment	PAK6	1.17
134	Early-onset posterior polar cataract	Enrichment	EPHA2	1.17
135	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies	Enrichment	RAC1	1.12
136	Arteriovenous malformation	Enrichment	RASA1	1.12
137	Congenital central hypoventilation syndrome	Enrichment	BDNF	1.12
138	Renal agenesis, bilateral	Enrichment	ROBO1	1.12
139	Myopathy, x-linked, with excessive autophagy	Enrichment	RASA1	1.08
140	Autosomal non-syndromic agammaglobulinemia	Enrichment	PIK3R1	1.08
141	Undetermined early-onset epileptic encephalopathy	Enrichment	LIMK1, NTRK2	1.08
142	Complex neurodevelopmental disorder	Enrichment	DPYSL5, PAK3, RAC3	1.04
143	Schizophrenia	Enrichment	RELN, RTN4R	1.04
144	Lip and oral cavity carcinoma	Enrichment	ABL1	1.01
145	Cataract	Enrichment	EPHA2	0.94
146	Pituitary stalk interruption syndrome	Enrichment	ROBO1	0.94
147	Congenital myopathy 4a, autosomal dominant	Enrichment	MYL2	0.91
148	Corpus callosum, agenesis of	Enrichment	DCC	0.91
149	Isolated corpus callosum agenesis	Enrichment	DCC	0.91
150	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome	Enrichment	DCC	0.91
151	Creatine phosphokinase, elevated serum	Enrichment	GDAP1	0.89
152	Isolated elevated serum creatine phosphokinase levels	Enrichment	GDAP1	0.89
153	Alzheimer disease, familial, 1	Enrichment	UNC5C	0.86
154	Cardiomyopathy, dilated, 1e	Enrichment	MYL2	0.86
155	Cataract 44	Enrichment	EPHA2	0.86
156	Early-onset nuclear cataract	Enrichment	EPHA2	0.84
157	Williams-beuren syndrome	Enrichment	LIMK1	0.80
158	Lissencephaly	Enrichment	RELN	0.78
159	Centronuclear myopathy	Enrichment	CFL2	0.78
160	Colorectal cancer	Enrichment	DCC, PIK3R1	0.76
161	Myocardial infarction	Enrichment	LRP8	0.76
162	Precursor t-cell acute lymphoblastic leukemia	Enrichment	ABL1	0.74
163	Familial atrial fibrillation	Enrichment	MYL4	0.73
164	Scoliosis	Enrichment	RELN	0.73
165	Tetralogy of fallot	Enrichment	ROBO1	0.70
166	Brugada syndrome	Enrichment	SEMA3A	0.70
167	Hirschsprung disease 1	Enrichment	DSCAM	0.65
168	Non-syndromic x-linked intellectual disability	Enrichment	ARHGEF6	0.57
169	Developmental and epileptic encephalopathy	Enrichment	ARHGEF15	0.57
170	Microcephaly	Enrichment	ABL1, PAK3	0.54
171	Benign epilepsy with centrotemporal spikes	Enrichment	RELN	0.52
172	Distal arthrogryposis	Enrichment	MYL11	0.52
173	Centralopathic epilepsy	Enrichment	RELN	0.51
174	West syndrome	Enrichment	NTRK2	0.50
175	Body mass index quantitative trait locus 11	Enrichment	BDNF	0.45
176	Spastic ataxia	Enrichment	DAB1	0.43
177	Myeloma, multiple	Enrichment	PIK3R2	0.41
178	Primary ovarian insufficiency	Enrichment	NTRK1	0.40
179	Dilated cardiomyopathy	Enrichment	MYL2	0.30
180	Ovarian cancer	Enrichment	NTRK1	0.23
181	Congenital nervous system abnormality	Enrichment	VLDLR	0.22
182	Nervous system disease	Enrichment	VLDLR	0.22
183	Autism spectrum disorder	Enrichment	DCC	0.21

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

Guidance Cues and Growth Cone Motility

Pathway Network for Guidance Cues and Growth Cone Motility

Member Pathways for Guidance Cues and Growth Cone Motility

Pathways in the Guidance Cues and Growth Cone Motility SuperPath

Associated Genes for Guidance Cues and Growth Cone Motility

Associated Disorders for Guidance Cues and Growth Cone Motility

Disorders associated with Guidance Cues and Growth Cone Motility SuperPath

STRING Interaction Network for Guidance Cues and Growth Cone Motility

Sources for Guidance Cues and Growth Cone Motility