Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock genes

No Pathway Network information available for Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock genes

Pathways in the Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock genes SuperPath

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

Disorders associated with Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock genes SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Advanced sleep phase syndromeEnrichmentPER2, PER35.08
2Rare genetic intellectual disabilityEnrichmentCREBBP, KMT2A3.55
3Advanced sleep phase syndrome, familial, 1EnrichmentPER22.77
4Advanced sleep phase syndrome, familial, 3EnrichmentPER32.77
5Immunodeficiency 42EnrichmentRORC2.77
6Delayed sleep phase disorderEnrichmentCRY12.77
7Menke-hennekam syndrome 1EnrichmentCREBBP2.77
8Acute myeloid leukemia with mll rearrangementEnrichmentKMT2A2.77
9Rubinstein-taybi syndrome due to 16p13.3 microdeletionEnrichmentCREBBP2.77
10Menke-hennekam syndromeEnrichmentCREBBP2.77
11Language disorderEnrichmentSIK12.77
12Thumb deformityEnrichmentCREBBP2.47
13Histiocytoma, angiomatoid fibrousEnrichmentCREB12.47
14Homocystinuria-megaloblastic anemia, cble typeEnrichmentPER32.47
15Hypothyroidism, congenital, nongoitrous, 6EnrichmentNR1D12.47
16Acute myeloid leukemia with kat6a-crebbp fusionEnrichmentCREBBP2.47
17Developmental and epileptic encephalopathy 30EnrichmentSIK12.47
18Intellectual developmental disorder with or without epilepsy or cerebellar ataxiaEnrichmentRORA2.47
19Acute myeloid leukemia with t(9;11)(p22;q23)EnrichmentKMT2A2.47
20Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)EnrichmentKMT2A2.47
21B-lymphoblastic leukemia/lymphoma with tEnrichmentKMT2A2.47
22Tethered spinal cord syndromeEnrichmentCREBBP2.29
23Intraocular pressure quantitative trait locusEnrichmentCREBBP2.29
24Melanoma of soft tissueEnrichmentCREB12.29
25Mixed phenotype acute leukemia with tEnrichmentKMT2A2.29
26Acute megakaryocytic leukemiaEnrichmentKMT2A2.07
27Kabuki syndrome 1EnrichmentKMT2A1.99
28Rubinstein-taybi syndrome 1EnrichmentCREBBP1.99
29Wiedemann-steiner syndromeEnrichmentKMT2A1.99
30Chromosome 16p13.3 deletion syndrome, proximalEnrichmentCREBBP1.99
31HypertrichosisEnrichmentCREBBP1.99
32Renal cell carcinoma with mit translocationsEnrichmentTFEB1.93
33Cornelia de lange syndrome 1EnrichmentKMT2A1.82
34Cornelia de lange syndromeEnrichmentKMT2A1.82
35Heart diseaseEnrichmentCREBBP1.63
36Corpus callosum, agenesis ofEnrichmentCREBBP1.60
37Isolated corpus callosum agenesisEnrichmentCREBBP1.60
38Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCREBBP1.60
39Early infantile developmental and epileptic encephalopathyEnrichmentSIK11.52
40Diffuse large b-cell lymphomaEnrichmentCREBBP1.50
41ScoliosisEnrichmentCREBBP1.40
42Leukemia, acute myeloidEnrichmentKMT2A1.18
43Benign epilepsy with centrotemporal spikesEnrichmentLOC1027244281.17
44Centralopathic epilepsyEnrichmentLOC1027244281.15
45West syndromeEnrichmentSIK11.14
46Myeloma, multipleEnrichmentCREBBP1.04
47AutismEnrichmentCREBBP0.94
48Congenital nervous system abnormalityEnrichmentCREBBP0.78
49Nervous system diseaseEnrichmentCREBBP0.78
50Autism spectrum disorderEnrichmentKMT2A0.77
51MicrocephalyEnrichmentKMT2A0.72
52Complex neurodevelopmental disorderEnrichmentRORA0.72

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