GDNF-Family Ligands and Receptor Interactions

Pathway network for the GDNF-Family Ligands and Receptor Interactions SuperPath

Sources:
  • QIAGEN
  • GeneGo (Thomson Reuters)

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

Disorders associated with GDNF-Family Ligands and Receptor Interactions SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1RasopathyEnrichmentHRAS, KRAS, MAP2K1, MAP2K2, MRAS, NRAS, RAF1, RRAS2, SOS1, SOS216.00
2Noonan syndrome and noonan-related syndromeEnrichmentHRAS, KRAS, MAP2K1, MAP2K2, NRAS, RAF1, SOS111.06
3Noonan syndrome 1EnrichmentHRAS, KRAS, MAP2K1, MAP2K2, MRAS, NRAS, RAF1, RRAS, RRAS2, SOS1, SOS210.63
4Noonan syndrome 3EnrichmentHRAS, KRAS, RAF1, SOS18.40
5Arteriovenous malformationEnrichmentHRAS, MAP2K1, PIK3CA, RASA17.43
6Lung non-small cell carcinomaEnrichmentHRAS, KRAS, MAP2K1, NRAS7.43
7Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, MAP2K1, PIK3CA, RASA17.21
8Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS, KRAS, NRAS6.84
9Cardiofaciocutaneous syndrome 1EnrichmentKRAS, MAP2K1, MAP2K26.84
10Cardiofaciocutaneous syndromeEnrichmentKRAS, MAP2K1, MAP2K26.84
11Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT3, PIK3CA, PIK3R26.53
12Nevus, epidermalEnrichmentHRAS, KRAS, NRAS5.90
13Pilomyxoid astrocytomaEnrichmentKRAS, NTRK2, RAF15.90
14Melanocytic nevus syndrome, congenitalEnrichmentHRAS, NRAS, RAF15.69
15Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K1, PIK3CA, RASA15.59
16Specific learning disabilityEnrichmentMAPK1, RPS6KA3, YWHAG5.23
17Juvenile myelomonocytic leukemiaEnrichmentKRAS, NRAS, RRAS5.10
18Ras-associated autoimmune leukoproliferative disorderEnrichmentKRAS, NRAS4.95
19Breast cancerEnrichmentAKT1, JUN, PIK3CA, RET, SHC14.78
20Langerhans cell histiocytosisEnrichmentMAP2K1, NRAS4.47
21Large congenital melanocytic nevusEnrichmentHRAS, NRAS4.47
22Colorectal cancerEnrichmentAKT1, PIK3CA, PIK3R1, RET, SRC4.47
23Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R14.27
24Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3CD, PIK3R14.27
25Immunodeficiency 14EnrichmentPIK3CD, PIK3R14.27
26Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentKRAS, NRAS4.17
27Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT3, PIK3R23.97
28Differentiated thyroid carcinomaEnrichmentHRAS, KRAS, NRAS3.90
29Breast adenocarcinomaEnrichmentAKT1, KRAS3.78
30Capillary malformations, congenitalEnrichmentPIK3CA, RASA13.75
31HemimegalencephalyEnrichmentAKT3, PIK3CA3.75
32Thyroid cancer, nonmedullary, 2EnrichmentHRAS, NRAS3.63
33Leukemia, chronic myeloidEnrichmentKRAS, NRAS3.63
34Follicular thyroid carcinomaEnrichmentHRAS, NRAS3.63
35Hirschsprung disease 1EnrichmentGDNF, NRTN, RET3.60
36Klippel-trenaunay-weber syndromeEnrichmentPIK3CA, RASA13.57
37Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.43
38Congenital central hypoventilation syndromeEnrichmentGDNF, RET3.20
39Cowden syndromeEnrichmentAKT1, PIK3CA3.20
40Renal agenesis, bilateralEnrichmentGFRA1, RET3.20
41Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3CD, PIK3R13.10
42Hereditary breast carcinomaEnrichmentAKT1, PIK3CA, RET3.06
43Ovarian cancerEnrichmentAKT1, MAP3K1, PIK3CA, RET3.04
44MeningiomaEnrichmentAKT1, PIK3CA2.94
45Lip and oral cavity carcinomaEnrichmentHRAS, PIK3CA2.94
46HypertelorismEnrichmentPIK3CA, RET, RPS6KA32.85
4746,xy partial gonadal dysgenesisEnrichmentMAP3K1, SOS12.80
48Anhidrosis, isolated, with normal sweat glandsEnrichmentITPR22.47
49Proteus syndromeEnrichmentAKT12.47
50Coffin-lowry syndromeEnrichmentRPS6KA32.47
51Oculoectodermal syndromeEnrichmentKRAS2.47
52Deafness, autosomal recessive 26EnrichmentGAB12.47
53Noonan syndrome 5EnrichmentRAF12.47
54Noonan syndrome 4EnrichmentSOS12.47
55Melorheostosis, isolatedEnrichmentMAP2K12.47
56Cardiomyopathy, dilated, 1nnEnrichmentRAF12.47
57Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.47
58Melanosis, neurocutaneousEnrichmentNRAS2.47
59Noonan syndrome 9EnrichmentSOS22.47
60Noonan syndrome 6EnrichmentNRAS2.47
61Ataxia-oculomotor apraxia 3EnrichmentPIK3R52.47
62Noonan syndrome 11EnrichmentMRAS2.47
63Noonan syndrome 13EnrichmentMAPK12.47
64Developmental and epileptic encephalopathy 58EnrichmentNTRK22.47
65Charcot-marie-tooth disease, demyelinating, type 1jEnrichmentITPR32.47
66Short syndromeEnrichmentPIK3R12.47
67Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.47
68Intellectual developmental disorder, x-linked 19EnrichmentRPS6KA32.47
69Cardiofaciocutaneous syndrome 2EnrichmentKRAS2.47
70MelorheostosisEnrichmentMAP2K12.47
71Leopard syndrome 2EnrichmentRAF12.47
72Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.47
73Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.47
74Autoinflammation, antibody deficiency, and immune dysregulationEnrichmentPLCG22.47
75Cowden syndrome 6EnrichmentAKT12.47
76Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.47
77Obesity, hyperphagia, and developmental delayEnrichmentNTRK22.47
78Familial cold autoinflammatory syndrome 3EnrichmentPLCG22.47
79Developmental and epileptic encephalopathy 56EnrichmentYWHAG2.47
80TrigonitisEnrichmentRAF12.47
81Symptomatic form of coffin-lowry syndrome in female carriersEnrichmentRPS6KA32.47
82Immunodeficiency 133 with ectodermal dysplasia with or without peripheral neuropathyEnrichmentITPR32.47
83Congenital pulmonary airway malformationEnrichmentKRAS2.47
84Phakomatosis pigmentokeratoticaEnrichmentHRAS2.47
85Distal 17p13.3 microdeletion syndromeEnrichmentYWHAE2.47
86Neurocutaneous melanocytosisEnrichmentNRAS2.47
87Hepatocellular carcinomaEnrichmentPIK3CA, RET2.41
88Multiple endocrine neoplasia, type iibEnrichmentRET2.37
89MacrodactylyEnrichmentPIK3CA2.37
90Cystic angiomatosis of bone, diffuseEnrichmentRASA12.37
91Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT22.37
92Megalencephaly, autosomal dominantEnrichmentPIK3CA2.37
93Cowden syndrome 5EnrichmentPIK3CA2.37
94Fetal encasement syndromeEnrichmentCHUK2.37
9546,xy sex reversal 6EnrichmentMAP3K12.37
96Cerebral cavernous malformations 4EnrichmentPIK3CA2.37
97Immunodeficiency 15bEnrichmentIKBKB2.37
98Immunodeficiency 15aEnrichmentIKBKB2.37
99Immunodeficiency 92EnrichmentREL2.37
100Intellectual developmental disorder with macrocephaly, seizures, and speech delayEnrichmentPAK12.37
101Renal hypodysplasia/aplasia 4EnrichmentGFRA12.37
102Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.37
103Hemifacial myohyperplasiaEnrichmentPIK3CA2.37
104Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.37
105Immunodeficiency 14b, autosomal recessiveEnrichmentPIK3CD2.37
106Hirschsprung disease 3EnrichmentGDNF2.37
107Thrombocytopenia 6EnrichmentSRC2.37
108Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.37
109Immunodeficiency 53EnrichmentRELB2.37
110Bartsocas-papas syndrome 2EnrichmentCHUK2.37
111Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.37
112HypospadiasEnrichmentPIK3CA2.37
113Capillary hemangiomaEnrichmentAKT32.37
114Thyroid cancerEnrichmentRET2.37
115Rare venous malformationEnrichmentPIK3CA2.37
116Gorham's diseaseEnrichmentRASA12.37
117Diaphragmatic eventrationEnrichmentPIK3CA2.37
118Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.37
119Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.37
120Rare combined vascular malformationEnrichmentPIK3CA2.37
121Cavernous lymphangiomaEnrichmentPIK3CA2.37
122Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.37
123Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.37
124Eccrine angiomatous hamartomaEnrichmentPIK3CA2.37
125Macrodactyly of toeEnrichmentPIK3CA2.37
126Gastrointestinal system diseaseEnrichmentRET2.37
127Akt2-related familial partial lipodystrophyEnrichmentAKT22.37
128Multiple endocrine neoplasiaEnrichmentRET2.37
129Bladder cancerEnrichmentHRAS, KRAS2.37
130Cerebral cavernous malformations 5EnrichmentMAP3K32.32
131Verrucous hemangiomaEnrichmentMAP3K32.32
132Non-immune hydrops fetalisEnrichmentHRAS, KRAS2.31
133Spinocerebellar ataxia 29EnrichmentITPR12.17
134Fibromatosis, gingival, 1EnrichmentSOS12.17
135Costello syndromeEnrichmentHRAS2.17
136Pulmonic stenosisEnrichmentSOS12.17
137Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2EnrichmentPIK3R52.17
138Histiocytoma, angiomatoid fibrousEnrichmentCREB12.17
139Encephalocraniocutaneous lipomatosisEnrichmentKRAS2.17
140Noonan syndrome 12EnrichmentRRAS22.17
141Intravascular large b-cell lymphomaEnrichmentBCL22.17
142Tafro syndromeEnrichmentMAP2K22.17
143Wooly hair nevusEnrichmentHRAS2.17
144Leukemia, acute myeloidEnrichmentKRAS, NRAS2.09
145Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.07
146Keratosis, seborrheicEnrichmentPIK3CA2.07
147Roifman-chitayat syndromeEnrichmentPIK3CD2.07
148Noonan syndrome 8EnrichmentPIK3CA2.07
149Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.07
150Immunodeficiency, common variable, 10EnrichmentNFKB22.07
151Myopia 28, autosomal recessiveEnrichmentDOK12.07
152Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.07
153Rela fusion-positive ependymomaEnrichmentRELA2.07
154Senior-loken syndrome 7EnrichmentAKT32.07
155Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.07
156Medullary thyroid carcinomaEnrichmentRET2.07
157Ectodermal dysplasia and immune deficiencyEnrichmentNFKBIA2.07
158Immune system diseaseEnrichmentPIK3CD2.07
159Bardet-biedl syndrome 16EnrichmentAKT32.07
160Common variable immunodeficiency 12EnrichmentNFKB12.07
161Gillespie syndromeEnrichmentITPR11.99
162Nuchal bleb, familialEnrichmentSOS11.99
163Miller-dieker lissencephaly syndromeEnrichmentYWHAE1.99
164Chromosome 17p13.3, centromeric, duplication syndromeEnrichmentYWHAE1.99
165High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL21.99
166SpermatocytomaEnrichmentHRAS1.99
167Melanoma of soft tissueEnrichmentCREB11.99
168Thyroid carcinoma, familial medullaryEnrichmentRET1.89
169Pompe disease, infantile-onsetEnrichmentPIK3CA1.89
170Nasopharyngeal carcinomaEnrichmentNFKBIA1.89
171Wieacker-wolff syndromeEnrichmentRASA11.89
172Gingival overgrowthEnrichmentRET1.89
173KeratoacanthomaEnrichmentPIK3CA1.89
174Diffuse gastric and lobular breast cancer syndromeEnrichmentKRAS1.87
175Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.87
176Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.87
177Spinocerebellar ataxia 15EnrichmentITPR11.87
178Lung sarcomatoid carcinomaEnrichmentKRAS1.87
179Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentYWHAZ1.87
180Noonan syndrome with multiple lentiginesEnrichmentRAF11.87
181Pilocytic astrocytomaEnrichmentKRAS1.87
182Epidermolytic nevusEnrichmentHRAS1.87
183Gingival fibromatosisEnrichmentSOS11.87
184Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentSOS21.87
185Type 2 diabetes mellitusEnrichmentAKT2, IRS11.86
186Myeloma, multipleEnrichmentKRAS, PIK3R21.81
187Undetermined early-onset epileptic encephalopathyEnrichmentNTRK2, YWHAG1.81
188Follicular lymphomaEnrichmentBCL21.77
189Endometrial stromal sarcomaEnrichmentYWHAE1.77
190Immunodeficiency, common variable, 1EnrichmentNFKB21.77
191Central hypoventilation syndrome, congenital, 1EnrichmentRET1.77
192Cerebrovascular diseaseEnrichmentPIK3CA1.77
193Familial cerebral cavernous malformationsEnrichmentPIK3CA1.77
194Haddad syndromeEnrichmentRET1.77
195Congenital generalized lipodystrophyEnrichmentFOS1.72
196Wilms tumor, aniridia, genitourinary anomalies, and impaired intellectual development syndromeEnrichmentBDNF1.70
197Spinocerebellar ataxia, autosomal recessive 16EnrichmentITPR11.70
198Lung squamous cell carcinomaEnrichmentKRAS1.70
199Kidney clear cell sarcomaEnrichmentYWHAE1.70
200Multiple endocrine neoplasia, type iiaEnrichmentRET1.67
201Gallbladder cancerEnrichmentKRAS1.63
202Overgrowth syndromeEnrichmentPIK3R11.63
203Histiocytoid hemangiomaEnrichmentFOS1.62
204Cowden syndrome 1EnrichmentPIK3CA1.60
205Telangiectasia, hereditary hemorrhagic, type 1EnrichmentRASA11.60
206Hemihyperplasia, isolatedEnrichmentPIK3CA1.60
207Hemangioma, capillary infantileEnrichmentRASA11.60
208Basal cell carcinoma 1EnrichmentRASA11.60
209Sporadic pheochromocytoma/secreting paragangliomaEnrichmentRET1.60
210Gastroesophageal refluxEnrichmentRPS6KA31.57
211Orthostatic intoleranceEnrichmentRPS6KA31.57
212MyelofibrosisEnrichmentSRC1.53
213Hereditary hemorrhagic telangiectasiaEnrichmentRASA11.53
214MegacolonEnrichmentAKT31.53
215Ventricular septal defectEnrichmentRPS6KA31.52
216Renal hypodysplasia/aplasia 1EnrichmentRET1.47
217Lennox-gastaut syndromeEnrichmentMAPK101.47
218HypothyroidismEnrichmentRET1.47
219Adult hepatocellular carcinomaEnrichmentPIK3CA1.42
220Congenital long qt syndromeEnrichmentITPR31.40
221Ciliary dyskinesia, primary, 3EnrichmentNFKB11.38
222PolymicrogyriaEnrichmentAKT31.38
223Aortic valve disease 1EnrichmentSOS11.36
224Protein-deficiency anemiaEnrichmentNRAS1.36
22546,xy complete gonadal dysgenesisEnrichmentMAP3K11.34
226Multiple sclerosisEnrichmentITPR11.33
227Lung cancer susceptibility 3EnrichmentKRAS1.33
228Anterior segment dysgenesisEnrichmentITPR11.30
229Lynch syndromeEnrichmentKRAS1.30
230Renal hypodysplasia/aplasia 3EnrichmentRET1.30
231RhabdomyosarcomaEnrichmentHRAS1.28
232Nk-cell enteropathyEnrichmentPIK3CB1.27
233OsteoporosisEnrichmentSRC1.23
234PheochromocytomaEnrichmentRET1.23
235Heart, malformation ofEnrichmentMAPK11.23
236Arteriovenous malformations of the brainEnrichmentKRAS1.20
237MicrocephalyEnrichmentMAPK1, YWHAG1.19
238GliosarcomaEnrichmentNFKBIA1.18
239Giant cell glioblastomaEnrichmentNFKBIA1.15
240Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.11
241Pancreatic cancerEnrichmentKRAS1.09
242Hydrops fetalis, nonimmuneEnrichmentHRAS1.07
243Endometrial cancerEnrichmentPIK3CA1.06
244Hereditary paraganglioma-pheochromocytoma syndromesEnrichmentRET1.06
245Long qt syndrome 1EnrichmentITPR31.01
246Lung cancerEnrichmentKRAS0.99
247Tetralogy of fallotEnrichmentRET0.98
248Familial hypertrophic cardiomyopathyEnrichmentRAF10.97
249Left ventricular noncompactionEnrichmentRAF10.95
250Non-syndromic x-linked intellectual disabilityEnrichmentRPS6KA30.94
251Prostate cancerEnrichmentPIK3CA0.93
252Severe combined immunodeficiencyEnrichmentIKBKB0.88
253Gastric cancerEnrichmentKRAS0.87
254West syndromeEnrichmentNTRK20.86
255Body mass index quantitative trait locus 11EnrichmentBDNF0.81
256Autosomal dominant non-syndromic intellectual disabilityEnrichmentYWHAZ0.81
257Spastic ataxiaEnrichmentITPR10.78
258Familial isolated dilated cardiomyopathyEnrichmentRAF10.78
259Hereditary breast ovarian cancer syndromeEnrichmentKRAS0.77
260Sensorineural hearing lossEnrichmentRET0.73
261ThrombocytopeniaEnrichmentSRC0.73
262Dilated cardiomyopathyEnrichmentRAF10.62
263Autism spectrum disorderEnrichmentMAP2K10.51
264Inherited cancer-predisposing syndromeEnrichmentRET0.36

Loading...
Loading...
Loading...