Non-genomic actions of 1,25 dihydroxyvitamin D3

No Pathway Network information available for Non-genomic actions of 1,25 dihydroxyvitamin D3

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

Disorders associated with Non-genomic actions of 1,25 dihydroxyvitamin D3 SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS, KRAS, NRAS6.70
2Behcet syndromeEnrichmentIFNGR1, NOD2, TLR4, TNFRSF1A6.18
3Nevus, epidermalEnrichmentHRAS, KRAS, NRAS5.76
4Common variable immunodeficiencyEnrichmentCD40LG, NFKB1, NFKB25.76
5Lung non-small cell carcinomaEnrichmentHRAS, KRAS, NRAS5.09
6Ras-associated autoimmune leukoproliferative disorderEnrichmentKRAS, NRAS4.86
7Noonan syndrome and noonan-related syndromeEnrichmentHRAS, KRAS, NRAS4.66
8Large congenital melanocytic nevusEnrichmentHRAS, NRAS4.38
9Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentKRAS, NRAS4.08
10Hepatitis bEnrichmentIFNAR2, IFNGR14.08
11Noonan syndrome 1EnrichmentHRAS, KRAS, NRAS4.08
12RasopathyEnrichmentHRAS, KRAS, NRAS3.91
13Differentiated thyroid carcinomaEnrichmentHRAS, KRAS, NRAS3.77
14Thyroid cancer, nonmedullary, 2EnrichmentHRAS, NRAS3.54
15Leukemia, chronic myeloidEnrichmentKRAS, NRAS3.54
16Noonan syndrome 3EnrichmentHRAS, KRAS3.54
17Follicular thyroid carcinomaEnrichmentHRAS, NRAS3.54
18Melanocytic nevus syndrome, congenitalEnrichmentHRAS, NRAS3.42
19Inflammatory bowel disease 1EnrichmentIL6, NOD23.31
20Juvenile myelomonocytic leukemiaEnrichmentKRAS, NRAS3.05
21Multiple sclerosisEnrichmentCYP27B1, TNFRSF1A2.91
22Human immunodeficiency virus type 1EnrichmentCCL2, IFNG2.69
23Arteriovenous malformations of the brainEnrichmentIL6, KRAS2.64
24Autoinflammatory diseaseEnrichmentNOD2, TNFRSF1A2.44
25Periodic fever, familial, autosomal dominantEnrichmentTNFRSF1A2.42
26Oculoectodermal syndromeEnrichmentKRAS2.42
27Helicobacter pylori infectionEnrichmentIFNGR12.42
28Lipodystrophy, congenital generalized, type 3EnrichmentCAV12.42
29Melanosis, neurocutaneousEnrichmentNRAS2.42
30Noonan syndrome 6EnrichmentNRAS2.42
31Blau syndromeEnrichmentNOD22.42
32Pulmonary hypertension, primary, 3EnrichmentCAV12.42
33Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.42
34Immunodeficiency 27aEnrichmentIFNGR12.42
35Immunodeficiency 15bEnrichmentIKBKB2.42
36Immunodeficiency 69EnrichmentIFNG2.42
37Noonan syndrome 13EnrichmentMAPK12.42
38Immunodeficiency 15aEnrichmentIKBKB2.42
39Immunodeficiency with hyper-igm, type 1EnrichmentCD40LG2.42
40Lipodystrophy, familial partial, type 7EnrichmentCAV12.42
41Cardiofaciocutaneous syndrome 2EnrichmentKRAS2.42
42Immunodeficiency 27bEnrichmentIFNGR12.42
43Spinocerebellar ataxia 14EnrichmentPRKCG2.42
44Immunodeficiency with hyper-igm, type 3EnrichmentCD402.42
45Immunodeficiency 31aEnrichmentSTAT12.42
46Multiple sclerosis 5EnrichmentTNFRSF1A2.42
47Autoinflammation, antibody deficiency, and immune dysregulationEnrichmentPLCG22.42
48Macular degeneration, age-related, 10EnrichmentTLR42.42
49Immunodeficiency 31bEnrichmentSTAT12.42
50Familial cold autoinflammatory syndrome 3EnrichmentPLCG22.42
51Tnf receptor-associated periodic fever syndromeEnrichmentTNFRSF1A2.42
52Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.42
53Immunodeficiency 53EnrichmentRELB2.42
54RicketsEnrichmentVDR2.42
55Congenital pulmonary airway malformationEnrichmentKRAS2.42
56Cd40 ligand deficiencyEnrichmentCD40LG2.42
57Phakomatosis pigmentokeratoticaEnrichmentHRAS2.42
58Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial ifngammar2 deficiencyEnrichmentIFNGR22.42
59Neurocutaneous melanocytosisEnrichmentNRAS2.42
60Bladder cancerEnrichmentHRAS, KRAS2.28
61Non-immune hydrops fetalisEnrichmentHRAS, KRAS2.22
62Scoliosis, isolated 1EnrichmentMAPK72.12
63Costello syndromeEnrichmentHRAS2.12
64Hypercalcemia, infantile, 1EnrichmentCYP24A12.12
65Encephalocraniocutaneous lipomatosisEnrichmentKRAS2.12
66Immunodeficiency 45EnrichmentIFNAR22.12
67Yao syndromeEnrichmentNOD22.12
68Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.12
69Immunodeficiency, common variable, 10EnrichmentNFKB22.12
70Immunodeficiency 31cEnrichmentSTAT12.12
71Immunodeficiency 127EnrichmentTNF2.12
72Intermittent hydrarthrosisEnrichmentTNFRSF1A2.12
73Autosomal recessive infantile hypercalcemiaEnrichmentCYP24A12.12
74Crohn's diseaseEnrichmentNOD22.12
75Common variable immunodeficiency 12EnrichmentNFKB12.12
76Wooly hair nevusEnrichmentHRAS2.12
77Systemic lupus erythematosusEnrichmentETS1, TNF2.03
78Leukemia, acute myeloidEnrichmentKRAS, NRAS2.01
79Jacobsen syndromeEnrichmentETS11.95
80Tuberous sclerosis 1EnrichmentIFNG1.95
81Vitamin d hydroxylation-deficient rickets, type 1aEnrichmentCYP27B11.95
82Langerhans cell histiocytosisEnrichmentNRAS1.95
83Psoriatic arthritisEnrichmentTNF1.95
84Hepatitis c virusEnrichmentIFNG1.95
85Tuberous sclerosis 2EnrichmentIFNG1.95
86Immunodeficiency 28EnrichmentIFNGR21.95
87Migraine without auraEnrichmentTNF1.95
88Immunodeficiency 44EnrichmentIFNAR21.95
89SpermatocytomaEnrichmentHRAS1.95
90Kaposi sarcomaEnrichmentIL61.83
91Cardiofaciocutaneous syndrome 1EnrichmentKRAS1.83
92Diffuse gastric and lobular breast cancer syndromeEnrichmentKRAS1.83
93Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.83
94Immunodeficiency, common variable, 1EnrichmentNFKB21.83
95Cardiofaciocutaneous syndromeEnrichmentKRAS1.83
96Lung sarcomatoid carcinomaEnrichmentKRAS1.83
97Hereditary ataxiaEnrichmentPRKCG1.83
98Pilocytic astrocytomaEnrichmentKRAS1.83
99Epidermolytic nevusEnrichmentHRAS1.83
100Cerebral malariaEnrichmentTNF1.83
101Systemic-onset juvenile idiopathic arthritisEnrichmentIL61.83
102Vitamin d-dependent rickets, type 2aEnrichmentVDR1.73
103Rheumatoid arthritis, systemic juvenileEnrichmentIL61.73
104Vascular dementiaEnrichmentTNF1.73
105Diffuse cutaneous systemic sclerosisEnrichmentCAV11.73
106Idiopathic aplastic anemiaEnrichmentIFNG1.73
107Myeloma, multipleEnrichmentKRAS, RXRA1.73
108Type 1 diabetes mellitusEnrichmentIL61.65
109Chronic mucocutaneous candidiasisEnrichmentSTAT11.65
110Limited sclerodermaEnrichmentCAV11.65
111Breast adenocarcinomaEnrichmentKRAS1.65
112Lung squamous cell carcinomaEnrichmentKRAS1.65
113Capillary malformation-arteriovenous malformation 1EnrichmentKRAS1.58
114Gallbladder cancerEnrichmentKRAS1.58
115Pilomyxoid astrocytomaEnrichmentKRAS1.58
116Breast cancerEnrichmentJUN, KRAS1.49
117Charge syndromeEnrichmentTNFRSF1A1.48
118Arteriovenous malformationEnrichmentHRAS1.48
119Myopathy, x-linked, with excessive autophagyEnrichmentHRAS1.43
120Ciliary dyskinesia, primary, 3EnrichmentNFKB11.43
121Aplastic anemiaEnrichmentIFNG1.43
122AsthmaEnrichmentTNF1.39
123Heritable pulmonary arterial hypertensionEnrichmentCAV11.39
124Specific learning disabilityEnrichmentMAPK11.39
125Lip and oral cavity carcinomaEnrichmentHRAS1.35
126Pulmonary disease, chronic obstructiveEnrichmentVDR1.32
127Alzheimer's diseaseEnrichmentTNF1.32
128Chromosome 1p36 deletion syndromeEnrichmentPRKCZ1.32
129Protein-deficiency anemiaEnrichmentNRAS1.32
130Lung cancer susceptibility 3EnrichmentKRAS1.29
131Lynch syndromeEnrichmentKRAS1.26
132RhabdomyosarcomaEnrichmentHRAS1.23
133Heart, malformation ofEnrichmentMAPK11.18
134Hepatocellular carcinomaEnrichmentVDR1.10
135Multisystem inflammatory syndrome in childrenEnrichmentIFNAR21.10
136MalariaEnrichmentTNF1.08
137Pancreatic cancerEnrichmentKRAS1.05
138Hydrops fetalis, nonimmuneEnrichmentHRAS1.03
139Lung cancerEnrichmentKRAS0.94
140Severe combined immunodeficiencyEnrichmentIKBKB0.93
141Type 2 diabetes mellitusEnrichmentIL60.83
142Gastric cancerEnrichmentKRAS0.82
143Hereditary breast carcinomaEnrichmentKRAS0.82
144Hereditary breast ovarian cancer syndromeEnrichmentKRAS0.73
145Colorectal cancerEnrichmentNRAS0.55
146Ovarian cancerEnrichmentKRAS0.50
147MicrocephalyEnrichmentMAPK10.43

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