ATF-2 transcription factor network

No Pathway Network information available for ATF-2 transcription factor network

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

Disorders associated with ATF-2 transcription factor network SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Inherited cancer-predisposing syndromeEnrichmentBRCA1, CDK4, NF1, PDGFRA, RB13.65
2Bladder cancerEnrichmentBRCA1, NF1, RB13.62
3Type 1 diabetes mellitusEnrichmentIL6, INS3.59
4Gastric cancerEnrichmentBRCA1, CDK4, NF13.11
5RhabdomyosarcomaEnrichmentBRCA1, NF12.70
6Breast cancerEnrichmentBRCA1, ESR1, JUN2.42
7Palmoplantar keratoderma, punctate type iiEnrichmentBRCA12.38
8Hypereosinophilic syndrome, idiopathicEnrichmentPDGFRA2.38
9Melanoma, cutaneous malignant 3EnrichmentCDK42.38
10Dermatitis, atopic, 4EnrichmentSOCS32.38
11Yt blood group antigenEnrichmentACHE2.38
12Pseudohypoaldosteronism, type iieEnrichmentCUL32.38
13Gist-plus syndromeEnrichmentPDGFRA2.38
14Immunodeficiency 69EnrichmentIFNG2.38
15Myeloid and lymphoid neoplasms associated with pdgfra rearrangementEnrichmentPDGFRA2.38
16Infant-type hemispheric gliomaEnrichmentBRCA12.38
17Camurati-engelmann disease 2EnrichmentTGFB22.38
18Neurodevelopmental disorder with or without autism or seizuresEnrichmentCUL32.38
19Trilateral retinoblastomaEnrichmentRB12.38
20Plexiform neurofibromaEnrichmentNF12.38
21NeurofibromaEnrichmentNF12.38
22NeurofibromatosisEnrichmentNF12.38
23Chromosome 17q11.2 deletion syndromeEnrichmentNF12.38
24Optic nerve gliomaEnrichmentNF12.38
25Hemoglobinopathy toms riverEnrichmentHBG22.38
26Primary peritoneal carcinomaEnrichmentBRCA12.38
27Lung oat cell carcinomaEnrichmentRB12.38
28Colorectal cancerEnrichmentBRCA1, CCND1, EP3002.24
29Cafe-au-lait spots, multipleEnrichmentNF12.08
30ArgininemiaEnrichmentARG12.08
31Quebec platelet disorderEnrichmentPLAU2.08
32Histiocytoma, angiomatoid fibrousEnrichmentCREB12.08
33Pseudohypoaldosteronism, type i, autosomal dominantEnrichmentCUL32.08
34Segawa syndrome, autosomal recessiveEnrichmentTH2.08
35Chromosome 13q14 deletion syndromeEnrichmentRB12.08
36Maturity-onset diabetes of the young, type 10EnrichmentINS2.08
37Cyanosis, transient neonatalEnrichmentHBG22.08
38Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalitiesEnrichmentKAT52.08
39HyperproinsulinemiaEnrichmentINS2.08
40Fanconi anemia, complementation group sEnrichmentBRCA12.08
41Menke-hennekam syndrome 2EnrichmentEP3002.08
42Chromosome 17q11.2 duplication syndrome, 1.4-mbEnrichmentNF12.08
43Intravascular large b-cell lymphomaEnrichmentBCL22.08
44Pancreatic cancer 4EnrichmentBRCA12.08
45Cleidocranial dysplasia 2EnrichmentCBFB2.08
46Diabetes mellitus, permanent neonatal, 4EnrichmentINS2.08
47Loeys-dietz syndrome 4EnrichmentTGFB22.08
48Bardet-biedl syndrome 9EnrichmentNF12.08
49Inflammatory breast carcinomaEnrichmentBRCA12.08
50Peritoneum cancerEnrichmentBRCA12.08
51Bilateral breast cancerEnrichmentBRCA12.08
52Chronic eosinophilic leukemiaEnrichmentPDGFRA2.08
53Brachydactyly-elbow wrist dysplasia syndromeEnrichmentMACROH2A12.08
54B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormalityEnrichmentPDGFRA2.08
55Familial retinoblastomaEnrichmentRB12.08
56Pleomorphic rhabdomyosarcomaEnrichmentNF12.08
57Ovarian cancerEnrichmentBRCA1, PDGFRA, RB12.06
58Type 1 diabetes mellitus 2EnrichmentINS1.90
59Dystonia, dopa-responsiveEnrichmentTH1.90
60RetinoblastomaEnrichmentRB11.90
61Pseudohypoaldosteronism, type iiaEnrichmentCUL31.90
62Tuberous sclerosis 1EnrichmentIFNG1.90
63Watson syndromeEnrichmentNF11.90
64Multicentric osteolysis, nodulosis, and arthropathyEnrichmentMMP21.90
65Osteogenic sarcomaEnrichmentRB11.90
66Hepatitis c virusEnrichmentIFNG1.90
67Neurofibromatosis, familial spinalEnrichmentNF11.90
68Estrogen resistanceEnrichmentESR11.90
69Tuberous sclerosis 2EnrichmentIFNG1.90
70Woolly hair, autosomal recessive 3EnrichmentRB11.90
71Chromosome 17q11.2 deletion syndrome, 1.4-mbEnrichmentNF11.90
72Hypotrichosis 8EnrichmentRB11.90
73High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL21.90
74Dedifferentiated liposarcomaEnrichmentCDK41.90
75Myxoid liposarcomaEnrichmentDDIT31.90
76Squamous cell carcinomaEnrichmentRB11.90
77Migraine without auraEnrichmentESR11.90
78Brain cancerEnrichmentNF11.90
79Bone osteosarcomaEnrichmentRB11.90
80Melanoma of soft tissueEnrichmentCREB11.90
81Well-differentiated liposarcomaEnrichmentCDK41.90
82Hereditary breast carcinomaEnrichmentBRCA1, ESR11.83
83Kaposi sarcomaEnrichmentIL61.78
84Small cell cancer of the lungEnrichmentRB11.78
85Polyposis syndrome, hereditary mixed, 1EnrichmentBRCA11.78
86Neurofibromatosis-noonan syndromeEnrichmentNF11.78
87CholangiocarcinomaEnrichmentBRCA11.78
88Lynch syndrome 4EnrichmentRB11.78
89Congenital generalized lipodystrophyEnrichmentFOS1.78
90Mantle cell lymphomaEnrichmentCCND11.78
91Arthrogryposis multiplex congenita 3, myogenic typeEnrichmentESR11.78
92Neonatal diabetes mellitusEnrichmentINS1.78
93Embryonal rhabdomyosarcomaEnrichmentNF11.78
94Pilocytic astrocytomaEnrichmentNF11.78
95Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)EnrichmentCBFB1.78
96Hereditary persistence of fetal hemoglobin-beta-thalassemia syndromeEnrichmentHBG21.78
97Systemic-onset juvenile idiopathic arthritisEnrichmentIL61.78
98Middle aortic syndromeEnrichmentNF11.78
99Alzheimer disease 2EnrichmentPLAU1.68
100Von hippel-lindau syndromeEnrichmentCCND11.68
101Rhabdomyosarcoma 2EnrichmentNF11.68
102Rheumatoid arthritis, systemic juvenileEnrichmentIL61.68
103Breast-ovarian cancer, familial 2EnrichmentBRCA11.68
104Rubinstein-taybi syndrome 2EnrichmentEP3001.68
105Follicular lymphomaEnrichmentBCL21.68
106Histiocytoid hemangiomaEnrichmentFOS1.68
107Hereditary persistence of fetal hemoglobin-sickle cell disease syndromeEnrichmentHBG21.68
108Primary hypereosinophilic syndromeEnrichmentPDGFRA1.68
109Idiopathic aplastic anemiaEnrichmentIFNG1.68
110Hereditary breast ovarian cancer syndromeEnrichmentBRCA1, NF11.65
111Myeloma, multipleEnrichmentCCND1, NF11.64
112Atrial septal defect 1EnrichmentTGFB21.60
113Rubinstein-taybi syndrome 1EnrichmentEP3001.60
114Chromosome 16p13.3 deletion syndrome, proximalEnrichmentEP3001.60
115Gastrointestinal stromal tumorEnrichmentPDGFRA1.54
116Fetal hemoglobin quantitative trait locus 1EnrichmentHBG21.48
117Ewing sarcomaEnrichmentNF11.48
118Permanent neonatal diabetes mellitusEnrichmentINS1.48
119Neurofibromatosis, type iEnrichmentNF11.43
120Charge syndromeEnrichmentEP3001.43
121Inflammatory bowel disease 1EnrichmentIL61.43
122Leukemia, acute lymphoblastic 3EnrichmentNF11.43
123Loeys-dietz syndromeEnrichmentTGFB21.43
124Marfan syndromeEnrichmentTGFB21.38
125Leukemia, chronic lymphocyticEnrichmentCCND11.38
126Aplastic anemiaEnrichmentIFNG1.38
127Migraine with or without aura 1EnrichmentESR11.34
128Diabetes mellitusEnrichmentINS1.34
129Uterine corpus cancerEnrichmentBRCA11.34
130Juvenile myelomonocytic leukemiaEnrichmentNF11.31
131Lip and oral cavity carcinomaEnrichmentRB11.31
132Breast-ovarian cancer, familial 1EnrichmentBRCA11.27
133Nk-cell enteropathyEnrichmentCUL31.27
134PheochromocytomaEnrichmentNF11.24
135Lung cancer susceptibility 3EnrichmentRB11.24
136Periventricular nodular heterotopiaEnrichmentBRCA11.24
137Cleft lip/palateEnrichmentPDGFRA1.24
138Polydactyly, postaxial, type a1EnrichmentEP3001.21
139Rare genetic intellectual disabilityEnrichmentEP3001.21
140Alzheimer disease, familial, 1EnrichmentPLAU1.16
141Melanoma, cutaneous malignant 1EnrichmentCDK41.16
142Human immunodeficiency virus type 1EnrichmentIFNG1.14
143Autism spectrum disorderEnrichmentCUL3, NF11.11
144Arteriovenous malformations of the brainEnrichmentIL61.11
145Ehlers-danlos syndromeEnrichmentTGFB21.11
146Maturity-onset diabetes of the youngEnrichmentINS1.09
147Endometrial cancerEnrichmentBRCA11.07
148Hereditary paraganglioma-pheochromocytoma syndromesEnrichmentNF11.07
149Myocardial infarctionEnrichmentESR11.05
150Skin diseaseEnrichmentNF11.05
151MalariaEnrichmentNOS21.03
152Pancreatic cancerEnrichmentBRCA11.00
153RasopathyEnrichmentNF10.98
154Prostate cancerEnrichmentBRCA10.94
155Lung cancerEnrichmentBRCA10.90
156Fanconi anemia, complementation group aEnrichmentBRCA10.86
157DystoniaEnrichmentTH0.86
158Type 2 diabetes mellitusEnrichmentIL60.79
159Familial thoracic aortic aneurysm and aortic dissectionEnrichmentTGFB20.77
160Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentPPARGC1A0.66
161MicrocephalyEnrichmentEP3000.39
162Complex neurodevelopmental disorderEnrichmentCUL30.39

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