AHR Pathway

No Pathway Network information available for AHR Pathway

Pathways in the AHR Pathway SuperPath

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

Disorders associated with AHR Pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Inherited cancer-predisposing syndromeEnrichmentAIP, RB1, SMARCA42.75
2Retinitis pigmentosa 85EnrichmentAHR2.73
3Orofacial cleft 10EnrichmentSUMO12.73
4Foveal hypoplasia 3EnrichmentAHR2.73
5Smarca4-deficient sarcoma of thoraxEnrichmentSMARCA42.73
6Ovarian small cell carcinomaEnrichmentSMARCA42.73
7Congenital anomalies of kidney and urinary tract 3EnrichmentNRIP12.73
8Trilateral retinoblastomaEnrichmentRB12.73
9Lung oat cell carcinomaEnrichmentRB12.73
10Spinocerebellar ataxia 17EnrichmentTBP2.43
11Rhabdoid tumor predisposition syndrome 2EnrichmentSMARCA42.43
12Chromosome 13q14 deletion syndromeEnrichmentRB12.43
13Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.43
14Menke-hennekam syndrome 2EnrichmentEP3002.43
15Rhabdoid tumor predisposition syndromeEnrichmentSMARCA42.43
16Rela fusion-positive ependymomaEnrichmentRELA2.43
17Bosch-boonstra-schaaf optic atrophy syndromeEnrichmentNR2F12.43
18Otosclerosis 12EnrichmentSMARCA42.43
19Coffin-siris syndrome 4EnrichmentSMARCA42.43
20AcromegalyEnrichmentAIP2.43
21Familial retinoblastomaEnrichmentRB12.43
22Null pituitary adenomaEnrichmentAIP2.43
23Familial isolated pituitary adenomaEnrichmentAIP2.43
24Silent pituitary adenomaEnrichmentAIP2.43
25GigantismEnrichmentAIP2.43
26RetinoblastomaEnrichmentRB12.26
27Osteogenic sarcomaEnrichmentRB12.26
28Estrogen resistanceEnrichmentESR12.26
29Pituitary adenoma 1, multiple typesEnrichmentAIP2.26
30Woolly hair, autosomal recessive 3EnrichmentRB12.26
31Hypotrichosis 8EnrichmentRB12.26
32Squamous cell carcinomaEnrichmentRB12.26
33Migraine without auraEnrichmentESR12.26
34Bone osteosarcomaEnrichmentRB12.26
35Growth hormone secreting pituitary adenomaEnrichmentAIP2.26
36Aip familial isolated pituitary adenomasEnrichmentAIP2.26
37Small cell cancer of the lungEnrichmentRB12.13
38Lynch syndrome 4EnrichmentRB12.13
39Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalitiesEnrichmentPOLR2A2.13
40Arthrogryposis multiplex congenita 3, myogenic typeEnrichmentESR12.13
41ProlactinomaEnrichmentAIP2.13
42Rubinstein-taybi syndrome 2EnrichmentEP3002.04
43Rubinstein-taybi syndrome 1EnrichmentEP3001.96
44Chromosome 16p13.3 deletion syndrome, proximalEnrichmentEP3001.96
45NeuroblastomaEnrichmentSMARCA41.83
46Charge syndromeEnrichmentEP3001.78
47Ventricular septal defectEnrichmentSMARCA41.78
48Migraine with or without aura 1EnrichmentESR11.70
49Atrial heart septal defectEnrichmentSMARCA41.70
50Interatrial communicationEnrichmentSMARCA41.70
51Lip and oral cavity carcinomaEnrichmentRB11.66
52Hypercholesterolemia, familial, 1EnrichmentSMARCA41.63
53Lung cancer susceptibility 3EnrichmentRB11.59
54Coffin-siris syndrome 1EnrichmentSMARCA41.56
55Polydactyly, postaxial, type a1EnrichmentEP3001.56
56Familial hypercholesterolemiaEnrichmentSMARCA41.56
57Rare genetic intellectual disabilityEnrichmentEP3001.56
58Cleft palate, isolatedEnrichmentSMARCA41.51
59Esophageal atresia/tracheoesophageal fistulaEnrichmentPOLR2B1.46
60Parkinson's diseaseEnrichmentTBP1.46
61Myocardial infarctionEnrichmentESR11.40
62Tooth agenesisEnrichmentSUMO11.40
63Parkinson disease, late-onsetEnrichmentTBP1.36
64Bladder cancerEnrichmentRB11.28
65CakutEnrichmentNRIP11.22
66Cerebral palsyEnrichmentSMARCA41.16
67Optic atrophy plus syndromeEnrichmentNR2F11.11
68Hereditary breast carcinomaEnrichmentESR11.11
69Myeloma, multipleEnrichmentNCOR21.01
70Breast cancerEnrichmentESR10.89
71Colorectal cancerEnrichmentEP3000.83
72Ovarian cancerEnrichmentRB10.77
73Autism spectrum disorderEnrichmentNR2F10.74
74MicrocephalyEnrichmentEP3000.69
75Retinitis pigmentosaEnrichmentAHR0.49

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