Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters

Pathway network for the Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters SuperPath

Sources:
  • Reactome

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

Disorders associated with Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Human immunodeficiency virus infectious diseaseDirect
2TuberculosisDirect
3Mednik syndromeEnrichmentAP1B1, AP1S14.91
4Keratitis-ichthyosis-deafness syndrome, autosomal recessiveEnrichmentAP1B12.69
5Hypocalciuric hypercalcemia, familial, type iiiEnrichmentAP2S12.69
6Immunodeficiency 43EnrichmentB2M2.69
7Knobloch syndrome 2EnrichmentPAK22.69
8Okt4 epitope deficiencyEnrichmentCD42.69
9Dialysis-related amyloidosisEnrichmentB2M2.69
10Usmani-riazuddin syndrome, autosomal recessiveEnrichmentAP1G12.69
11Immunodeficiency 25EnrichmentCD2472.69
12Immunodeficiency 40EnrichmentDOCK22.69
13Birdshot chorioretinopathyEnrichmentHLA-A2.69
14Psoriasis 15, pustularEnrichmentAP1S32.69
15Immunodeficiency 123 with hpv-related verrucosisEnrichmentCD282.69
16Immunodeficiency 22EnrichmentLCK2.69
17Usmani-riazuddin syndrome, autosomal dominantEnrichmentAP1G12.69
18Immunodeficiency 79EnrichmentCD42.69
19Amyloidosis, hereditary systemic 6EnrichmentB2M2.69
20Autoinflammation with pulmonary and cutaneous vasculitisEnrichmentHCK2.69
21Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.69
22Severe combined immunodeficiencyEnrichmentCD247, LCK2.68
23Severe cutaneous adverse reactionEnrichmentHLA-A2.38
24Schuurs-hoeijmakers syndromeEnrichmentPACS12.38
25Psoriasis 14, pustularEnrichmentAP1S32.38
26Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.38
27Periventricular nodular heterotopia 8EnrichmentARF12.38
28Pettigrew syndromeEnrichmentAP1S22.38
29Intellectual developmental disorder, autosomal dominant 60, with seizuresEnrichmentAP2M12.38
30Mycosis fungoidesEnrichmentCD282.21
31T-b+ severe combined immunodeficiency due to cd3delta/cd3epsilon/cd3zetaEnrichmentCD2472.21
32Saczary syndromeEnrichmentCD282.21
33Knobloch syndromeEnrichmentPAK22.08
34Immunodeficiency by defective expression of mhc class iEnrichmentB2M2.08
35Amyloidosis, hereditary systemic 2EnrichmentB2M1.99
36Knobloch syndrome 1EnrichmentPAK21.99
37Oligoarticular juvenile idiopathic arthritisEnrichmentCD2471.84
38Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentCD2471.84
39Lymphoma, non-hodgkin, familialEnrichmentB2M1.79
40Myoclonic-atonic epilepsyEnrichmentAP2M11.73
41Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.73
42Periventricular nodular heterotopiaEnrichmentARF11.54
43Severe covid-19EnrichmentHLA-A1.23
44Complex neurodevelopmental disorderEnrichmentAP1G10.64

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