Retrograde transport at the Trans-Golgi-Network

No Pathway Network information available for Retrograde transport at the Trans-Golgi-Network

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

Disorders associated with Retrograde transport at the Trans-Golgi-Network SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Congenital disorder of glycosylation, type iilEnrichmentCOG62.44
2Congenital disorder of glycosylation, type iijEnrichmentCOG42.44
3Congenital disorder of glycosylation, type iiqEnrichmentCOG22.44
4Developmental and epileptic encephalopathy 107EnrichmentNAPB2.44
5Saul-wilson syndromeEnrichmentCOG42.44
6Shaheen syndromeEnrichmentCOG62.44
7Cog4-congenital disorder of glycosylationEnrichmentCOG42.44
8Pontocerebellar hypoplasia, type 13EnrichmentVPS512.44
9Congenital disorder of glycosylation, type iibbEnrichmentCOG32.44
10Cog6-congenital disorder of glycosylationEnrichmentCOG62.44
11Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndromeEnrichmentCOG62.44
12Amyotrophy, hereditary neuralgicEnrichmentNAPB2.14
13Congenital disorder of glycosylation, type iihEnrichmentCOG82.14
14Catifa syndromeEnrichmentRIC12.14
15Developmental and epileptic encephalopathy 96EnrichmentNSF2.14
16Cog8-congenital disorder of glycosylationEnrichmentCOG82.14
17Pelizaeus-merzbacher diseaseEnrichmentRAB9B1.97
18Spastic paraplegia 2, x-linkedEnrichmentRAB9B1.97
19Congenital disorder of glycosylation, type iigEnrichmentCOG11.97
20Cog7-congenital disorder of glycosylationEnrichmentCOG71.97
21Pelizeaus-merzbacher spectrum disorderEnrichmentRAB9B1.97
22Pseudohypoparathyroidism, type ibEnrichmentSTX161.84
23Congenital disorder of glycosylation, type iiiEnrichmentCOG51.84
24Cog5-congenital disorder of glycosylationEnrichmentCOG51.84
25Pontocerebellar hypoplasia, type 2dEnrichmentVPS531.75
26Pontocerebellar hypoplasia, type 2eEnrichmentVPS531.60
27Immunodeficiency 47EnrichmentCOG71.54
28Cleft lip/palateEnrichmentRIC11.31
29Pontocerebellar hypoplasiaEnrichmentVPS531.20
30Hepatocellular carcinomaEnrichmentIGF2R1.12
31Auditory neuropathyEnrichmentRAB9B1.05
32Hereditary spastic paraplegiaEnrichmentRAB9B0.85
33Primary ovarian insufficiencyEnrichmentIGF2R0.72

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