Trafficking of AMPA receptors

Pathway network for the Trafficking of AMPA receptors SuperPath

Sources:
  • Reactome

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

Disorders associated with Trafficking of AMPA receptors SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Autosomal dominant non-syndromic intellectual disabilityEnrichmentCACNG2, CAMK2A, CAMK2B, EPB41L1, GRIA17.06
2Intellectual developmental disorder, x-linked, syndromic, wu typeEnrichmentGRIA33.53
3Neurodevelopmental disorder with language impairment and behavioral abnormalitiesEnrichmentGRIA23.53
4Neurodevelopmental disorder with or without seizures and gait abnormalitiesEnrichmentGRIA43.53
5Intellectual developmental disorder, autosomal dominant 67EnrichmentGRIA13.53
6Intellectual developmental disorder, autosomal recessive 76EnrichmentGRIA13.53
7Syndromic x-linked intellectual disability 94EnrichmentGRIA33.53
8Gria2-related neurodevelopmental disorderEnrichmentGRIA23.53
9Hypocalciuric hypercalcemia, familial, type iiiEnrichmentAP2S12.90
10Intellectual developmental disorder, x-linked 58EnrichmentTSPAN72.90
11Spinocerebellar ataxia 14EnrichmentPRKCG2.90
12Fraser syndrome 3EnrichmentGRIP12.90
13Deafness, autosomal dominant 22EnrichmentMYO62.64
14Chromosome 20q11-q12 deletion syndromeEnrichmentEPB41L12.64
15Accelerated tumor formationEnrichmentMDM22.64
16Intellectual developmental disorder, autosomal recessive 63EnrichmentCAMK2A2.64
17Intellectual developmental disorder, autosomal dominant 54EnrichmentCAMK2B2.64
18Lessel-kubisch syndromeEnrichmentMDM22.64
19Deafness, autosomal recessive 37EnrichmentMYO62.64
20Intellectual developmental disorder, autosomal dominant 10EnrichmentCACNG22.64
21Intellectual developmental disorder, autosomal dominant 53EnrichmentCAMK2A2.64
22Intellectual developmental disorder, autosomal dominant 59EnrichmentCAMK2G2.64
23Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndromeEnrichmentMYO62.64
24Autosomal dominant nonsyndromic hearing loss 22EnrichmentMYO62.64
25Developmental and epileptic encephalopathy 96EnrichmentNSF2.60
26Intellectual developmental disorder, autosomal dominant 60, with seizuresEnrichmentAP2M12.60
27DystoniaEnrichmentCAMK2B, GRIA32.54
28Vulto-van silfhout-de vries syndromeEnrichmentDLG42.34
29Hereditary ataxiaEnrichmentPRKCG2.30
30Heart defects, congenital, and other congenital anomaliesEnrichmentDLG42.16
31Intellectual developmental disorder, autosomal dominant 62EnrichmentDLG42.16
32Dedifferentiated liposarcomaEnrichmentMDM22.16
33Neurodevelopmental disorder with hypotonia and impaired expressive language and with or without seizuresEnrichmentDLG42.16
34Dlg4-related synaptopathyEnrichmentDLG42.16
35Well-differentiated liposarcomaEnrichmentMDM22.16
36Fraser syndrome 1EnrichmentGRIP12.13
37Acyl-coa dehydrogenase, very long-chain, deficiency ofEnrichmentDLG42.04
38Male infertility due to globozoospermiaEnrichmentPICK12.00
39Developmental and epileptic encephalopathyEnrichmentGRIA31.98
40Myoclonic-atonic epilepsyEnrichmentAP2M11.95
41West syndromeEnrichmentGRIA31.89
42Li-fraumeni syndromeEnrichmentMDM21.87
43Epidermolysis bullosa, junctional 5b, with pyloric atresiaEnrichmentMYO61.87
44Body mass index quantitative trait locus 11EnrichmentGRIA41.83
45Autosomal recessive non-syndromic intellectual disabilityEnrichmentGRIA11.77
46Cleft lip/palateEnrichmentDLG11.50
47Autism spectrum disorderEnrichmentGRIA11.50
48Complex neurodevelopmental disorderEnrichmentDLG4, GRIA41.49
49Non-syndromic x-linked intellectual disabilityEnrichmentTSPAN71.35
50Ear malformationEnrichmentMYO61.27
51Non-syndromic genetic deafnessEnrichmentMYO61.10
52Nonsyndromic hearing lossEnrichmentMYO61.04
53Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentMYO60.95
54AutismEnrichmentCAMK2G0.82
55Rare genetic deafnessEnrichmentMYO60.78
56Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentMYO60.73
57Congenital nervous system abnormalityEnrichmentCAMK2B0.67
58Nervous system diseaseEnrichmentCAMK2B0.67
59MicrocephalyEnrichmentCAMK2B0.61

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