Transcription factor regulation in adipogenesis

No Pathway Network information available for Transcription factor regulation in adipogenesis

Pathways in the Transcription factor regulation in adipogenesis SuperPath

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

Disorders associated with Transcription factor regulation in adipogenesis SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Type 2 diabetes mellitusEnrichmentIL6, INSR, IRS1, IRS2, PPARG, SLC2A410.21
2Leptin deficiency or dysfunctionEnrichmentLEP, PPARG4.82
3Donohue syndromeEnrichmentINSR2.79
4Hyperinsulinemic hypoglycemia, familial, 5EnrichmentINSR2.79
5Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalitiesEnrichmentINSR2.79
6Diabetes mellitus, insulin-resistant, with acanthosis nigricansEnrichmentINSR2.79
7Glucocorticoid resistance, generalizedEnrichmentNR3C12.79
8Congenital anomalies of kidney and urinary tract 3EnrichmentNRIP12.79
9Pparg-associated congenital generalized lipodystrophyEnrichmentPPARG2.79
10Acute myeloid leukemia with mutated cebpaEnrichmentCEBPA2.79
11Galactosemia iiEnrichmentNR3C12.49
12Phosphoenolpyruvate carboxykinase deficiency, mitochondrialEnrichmentPCK22.49
13Robinow-sorauf syndromeEnrichmentTWIST12.49
14Carotid intimal medial thickness 1EnrichmentPPARG2.49
15Histiocytoma, angiomatoid fibrousEnrichmentCREB12.49
16Hyperinsulinemic hypoglycemia, familial, 4EnrichmentINSR2.49
17Sweeney-cox syndromeEnrichmentTWIST12.49
18Immunodeficiency 127EnrichmentTNF2.49
19Familial partial lipodystrophyEnrichmentPPARG2.49
20Non-syndromic sagittal craniosynostosisEnrichmentTWIST12.49
21Craniosynostosis 1EnrichmentTWIST12.31
22Myoglobinuria, acute recurrent, autosomal recessiveEnrichmentLPIN12.31
23Psoriatic arthritisEnrichmentTNF2.31
24Adiponectin deficiencyEnrichmentADIPOQ2.31
25Migraine without auraEnrichmentTNF2.31
26Phosphoenolpyruvate carboxykinase deficiencyEnrichmentPCK22.31
27Melanoma of soft tissueEnrichmentCREB12.31
28Kaposi sarcomaEnrichmentIL62.19
29Lipodystrophy, familial partial, type 3EnrichmentPPARG2.19
30Saethre-chotzen syndromeEnrichmentTWIST12.19
31Congenital generalized lipodystrophyEnrichmentPPARG2.19
32Hereditary recurrent myoglobinuriaEnrichmentLPIN12.19
33Cerebral malariaEnrichmentTNF2.19
34Non-syndromic bicoronal craniosynostosisEnrichmentTWIST12.19
35Systemic-onset juvenile idiopathic arthritisEnrichmentIL62.19
36Rhabdomyosarcoma 2EnrichmentFOXO12.09
37Rheumatoid arthritis, systemic juvenileEnrichmentIL62.09
38Vascular dementiaEnrichmentTNF2.09
39Inherited acute myeloid leukemiaEnrichmentCEBPA2.09
40Acute myeloid leukemia with t(8;21)(q22;q22) translocationEnrichmentCEBPA2.09
41Type 1 diabetes mellitusEnrichmentIL62.01
4246,xy disorder of sex developmentEnrichmentINSR2.01
43Inflammatory bowel disease 1EnrichmentIL61.84
44Primary hyperaldosteronismEnrichmentNR3C11.84
45AsthmaEnrichmentTNF1.75
46Alzheimer's diseaseEnrichmentTNF1.68
47GliosarcomaEnrichmentPPARG1.59
48Giant cell glioblastomaEnrichmentPPARG1.56
49Arteriovenous malformations of the brainEnrichmentIL61.52
50Diffuse large b-cell lymphomaEnrichmentFOXO11.52
51MalariaEnrichmentTNF1.44
52Differentiated thyroid carcinomaEnrichmentPPARG1.34
53CakutEnrichmentNRIP11.27
54Systemic lupus erythematosusEnrichmentTNF1.21
55Leukemia, acute myeloidEnrichmentCEBPA1.20
56Body mass index quantitative trait locus 11EnrichmentPPARG1.11
57Myeloma, multipleEnrichmentRXRA1.06
58Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentPPARGC1A1.05
59Colorectal cancerEnrichmentPPARG0.88
60Inherited cancer-predisposing syndromeEnrichmentCEBPA0.71

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