Budding and maturation of HIV virion

Pathway network for the Budding and maturation of HIV virion SuperPath

Sources:
  • Reactome

Gene overlap in member pathways for Budding and maturation of HIV virion SuperPath

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

Disorders associated with Budding and maturation of HIV virion SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Human immunodeficiency virus infectious diseaseDirect
2Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmiaEnrichmentHDAC62.79
3Joubert syndrome 8EnrichmentARL13B2.79
4Microcephalic osteodysplastic primordial dwarfism, type iiEnrichmentPCNT2.79
5Danon diseaseEnrichmentLAMP22.79
6Parkinson disease 7, autosomal recessive early-onsetEnrichmentPARK72.79
7Sickle cell-beta-thalassemia disease syndromeEnrichmentHBB2.79
8Hemoglobin c-beta-thalassemia syndromeEnrichmentHBB2.79
9Aquagenic palmoplantar keratodermaEnrichmentCFTR2.79
10Sickle cell s-o arab diseaseEnrichmentHBB2.79
11Sickle cell-beta zero-thalassemiaEnrichmentHBB2.79
12Sickle cell s-d punjab diseaseEnrichmentHBB2.79
13Premature agingEnrichmentVIM2.79
14Sickle cell s-c diseaseEnrichmentHBB2.79
15Sickle cell s-e diseaseEnrichmentHBB2.79
16Homozygous hemoglobin o arab diseaseEnrichmentHBB2.79
17Sickle cell s-other specified hemoglobin variantEnrichmentHBB2.79
18Cataract 31, multiple typesEnrichmentCHMP4B2.63
19Spastic paraplegia 53, autosomal recessiveEnrichmentVPS37A2.63
20Developmental and epileptic encephalopathy 115EnrichmentSNF82.63
21Spastic paraplegia 80, autosomal dominantEnrichmentUBAP12.63
22Neurodevelopmental disorder plus optic atrophyEnrichmentSNF82.63
23Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1EnrichmentPARK72.49
24Alexander diseaseEnrichmentGFAP2.49
25Spermatogenic failure, y-linked, 2EnrichmentCFTR2.49
26Spastic paraplegia, intellectual disability, nystagmus, and obesityEnrichmentGFAP2.49
27Cataract 30EnrichmentVIM2.49
28Hemoglobin lepore-beta-thalassemia syndromeEnrichmentHBB2.49
29Sickle cell s-lepore diseaseEnrichmentHBB2.49
30Submucosal cleft palateEnrichmentUBB2.49
31Cleft hard palateEnrichmentUBB2.49
32Spastic paraplegia 12, autosomal dominantEnrichmentUBAP12.33
33Cimdag syndromeEnrichmentVPS4A2.33
34Uvula, bifidEnrichmentUBB2.31
35Nuchal bleb, familialEnrichmentCFTR2.31
36Cleft soft palateEnrichmentUBB2.31
37Hemoglobin e diseaseEnrichmentHBB2.31
38Sickle cell-hemoglobin c diseaseEnrichmentHBB2.31
39Hemoglobin d diseaseEnrichmentHBB2.31
40Delta beta-thalassemiaEnrichmentHBB2.31
41Unstable hemoglobin diseaseEnrichmentHBB2.31
42Hemoglobin e/beta thalassemia diseaseEnrichmentHBB2.31
43Sickle cell diseaseEnrichmentHBB2.19
44Beta-thalassemia, dominant inclusion body typeEnrichmentHBB2.19
45Erythrocytosis, familial, 6EnrichmentHBB2.19
46Beta-thalassemia intermediaEnrichmentHBB2.19
47HemoglobinopathyEnrichmentHBB2.19
48Idiopathic bronchiectasisEnrichmentCFTR2.19
49Hemoglobin c diseaseEnrichmentHBB2.19
50Hereditary persistence of fetal hemoglobin-beta-thalassemia syndromeEnrichmentHBB2.19
51Methemoglobinemia, beta-globin typeEnrichmentHBB2.19
52ThalassemiaEnrichmentHBB2.09
53Histiocytoid hemangiomaEnrichmentVIM2.09
54Hereditary persistence of fetal hemoglobin-sickle cell disease syndromeEnrichmentHBB2.09
55Dentin dysplasia, type iEnrichmentVPS4B2.03
56Metachromatic leukodystrophyEnrichmentGFAP2.01
57Parkinson disease 6, autosomal recessive early-onsetEnrichmentPARK72.01
58Methemoglobinemia, beta typeEnrichmentHBB2.01
59Autosomal dominant secondary polycythemiaEnrichmentHBB2.01
60Beta-thalassemiaEnrichmentHBB1.95
61Beta-thalassemia majorEnrichmentHBB1.95
62Hemolytic anemiaEnrichmentHBB1.95
63Cataract 6, multiple typesEnrichmentCHMP4B1.93
64Heinz body anemiasEnrichmentHBB1.89
65Fetal hemoglobin quantitative trait locus 1EnrichmentHBB1.89
66Heinz body anemiaEnrichmentHBB1.89
67Bronchiectasis with or without elevated sweat chloride 1EnrichmentCFTR1.84
68Vas deferens, congenital bilateral aplasia ofEnrichmentCFTR1.84
69Alpha-thalassemiaEnrichmentHBB1.84
70Cataract 30, multiple typesEnrichmentVIM1.79
71Semantic dementiaEnrichmentCHMP2B1.79
72Early-onset posterior polar cataractEnrichmentCHMP4B1.73
73Early-onset parkinson's diseaseEnrichmentPARK71.71
74Protein-deficiency anemiaEnrichmentHBB1.68
75Progressive non-fluent aphasiaEnrichmentCHMP2B1.68
76Behavioral variant of frontotemporal dementiaEnrichmentCHMP2B1.68
77Seckel syndromeEnrichmentPCNT1.65
78Hereditary chronic pancreatitisEnrichmentCFTR1.65
79Atypical hemolytic-uremic syndromeEnrichmentHBB1.62
80Lynch syndromeEnrichmentCFTR1.62
81Pancreatitis, hereditaryEnrichmentCFTR1.56
82MalariaEnrichmentHBB1.44
83ScoliosisEnrichmentGFAP1.42
84Williams-beuren syndromeEnrichmentVPS37D1.34
85Isolated joubert syndromeEnrichmentARL13B1.32
86Cystic fibrosisEnrichmentCFTR1.30
87Familial hypertrophic cardiomyopathyEnrichmentLAMP21.28
88Male infertilityEnrichmentCFTR1.27
89Left ventricular noncompactionEnrichmentLAMP21.26
90Hypertrophic cardiomyopathyEnrichmentLAMP21.17
91Joubert syndrome 1EnrichmentARL13B1.11
92Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentCFTR1.06
93Dilated cardiomyopathyEnrichmentLAMP20.91
94Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentCHMP2B0.89
95Retinitis pigmentosaEnrichmentIFT880.53

Loading...
Loading...
Loading...