Initiation of transcription and translation elongation at the HIV-1 LTR

No Pathway Network information available for Initiation of transcription and translation elongation at the HIV-1 LTR

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

Disorders associated with Initiation of transcription and translation elongation at the HIV-1 LTR SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Rubinstein-taybi syndrome 1EnrichmentCREBBP, EP3004.09
2Chromosome 16p13.3 deletion syndrome, proximalEnrichmentCREBBP, EP3004.09
3Rare genetic intellectual disabilityEnrichmentCREBBP, EP3003.26
4Chromosome 2q37 deletion syndromeEnrichmentHDAC42.63
5Auriculocondylar syndrome 4EnrichmentHDAC92.63
6Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.63
7Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.63
8Cornelia de lange syndrome 5EnrichmentHDAC82.63
9Menke-hennekam syndrome 1EnrichmentCREBBP2.63
10Neurodevelopmental disorder with central hypotonia and dysmorphic faciesEnrichmentHDAC42.63
11Rubinstein-taybi syndrome due to 16p13.3 microdeletionEnrichmentCREBBP2.63
12Menke-hennekam syndromeEnrichmentCREBBP2.63
13Thumb deformityEnrichmentCREBBP2.33
14Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.33
15Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.33
16Syndactyly, type iiiEnrichmentHDAC82.33
17Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.33
18Menke-hennekam syndrome 2EnrichmentEP3002.33
19Wilson-turner syndromeEnrichmentHDAC82.33
20Rela fusion-positive ependymomaEnrichmentRELA2.33
21Acute myeloid leukemia with kat6a-crebbp fusionEnrichmentCREBBP2.33
22Ectodermal dysplasia and immune deficiencyEnrichmentNFKBIA2.33
23Joint contractures, osteochondromas, and b-cell lymphomaEnrichmentNFATC22.33
24Common variable immunodeficiency 12EnrichmentNFKB12.33
25Nasopharyngeal carcinomaEnrichmentNFKBIA2.15
26Tethered spinal cord syndromeEnrichmentCREBBP2.15
27Intraocular pressure quantitative trait locusEnrichmentCREBBP2.15
28Myeloma, multipleEnrichmentCREBBP, HDAC42.12
29Rubinstein-taybi syndrome 2EnrichmentEP3001.93
30Wolf-hirschhorn syndromeEnrichmentNELFA1.85
31HypertrichosisEnrichmentCREBBP1.85
32Common variable immunodeficiencyEnrichmentNFKB11.79
33Fanconi anemia, complementation group cEnrichmentHDAC81.73
34Cornelia de lange syndrome 1EnrichmentHDAC81.68
35Charge syndromeEnrichmentEP3001.68
36Cornelia de lange syndromeEnrichmentHDAC81.68
37Ciliary dyskinesia, primary, 3EnrichmentNFKB11.63
38Atrial heart septal defectEnrichmentHDAC81.59
39Interatrial communicationEnrichmentHDAC81.59
40Heart diseaseEnrichmentCREBBP1.49
41MicrocephalyEnrichmentEP300, HDAC81.47
42Polydactyly, postaxial, type a1EnrichmentEP3001.46
43Corpus callosum, agenesis ofEnrichmentCREBBP1.46
44Isolated corpus callosum agenesisEnrichmentCREBBP1.46
45Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCREBBP1.46
46GliosarcomaEnrichmentNFKBIA1.43
47Giant cell glioblastomaEnrichmentNFKBIA1.40
48Polycystic kidney diseaseEnrichmentHDAC81.38
49Diffuse large b-cell lymphomaEnrichmentCREBBP1.36
50Cardiomyopathy, dilated, 1aEnrichmentNFATC21.31
51ScoliosisEnrichmentCREBBP1.26
52Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA0.95
53Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA0.91
54AutismEnrichmentCREBBP0.80
55Colorectal cancerEnrichmentEP3000.73
56Congenital nervous system abnormalityEnrichmentCREBBP0.65
57Nervous system diseaseEnrichmentCREBBP0.65

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