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Entry Name Description Category Pathway Gene
H02715 Neurodevelopmental disorder with defects of ubiquitin-proteasome system The ubiquitin-proteasome system (UPS) is the major proteolytic system that controls protein degradation and it regulates many cellular processes, such as cell division, gene expression and signal transduction ... Congenital malformation (NEDSG) UFC1 [HSA:51506] [KO:K12165]
(NDHSAL) HECW2 [HSA:57520] [KO:K12168]
(NEDAUS) CUL3 [HSA:8452] [KO:K03869]
(NEDAMSS) IRF2BPL [HSA:64207] [KO:K22383]
(NEDHMS) UBE4A [HSA:9354] [KO:K10596]
(NEDSMB) UBE3C [HSA:9690] [KO:K10589]
(NEDSSCC) HECTD4 [HSA:283450] [KO:K17849]
(NEDLBF) UBAP2L [HSA:9898] [KO:K26545]
(NSDVS1/2) SPOP [HSA:8405] [KO:K10523]
(NEDJED) FBXW11 [HSA:23291] [KO:K03362]
(BURHAS) SIAH1 [HSA:6477] [KO:K04506]
(NEDFIH) NAE1 [HSA:8883] [KO:K04532]
(MCAND) OTUD5 [HSA:55593] [KO:K12655]
(NEDHS) OTUD7A [HSA:161725] [KO:K11860]
(NEDMHAL) PSMB1 [HSA:5689] [KO:K02732]
(STISS) PSMD12 [HSA:5718] [KO:K03035]
(BKAH) PSMC1 [HSA:5700] [KO:K03062]
(CAFDADD) TRAF7 [HSA:84231] [KO:K10646]
(NEDBES) FEM1B [HSA:10116] [KO:K10349]
(TYMAS) FBXO22 [HSA:26263] [KO:K10302]
(NEDSBH) UBR5 [HSA:51366] [KO:K10593]
(YKNS) PSMC5 [HSA:5705] [KO:K03066]
(EBNDS) PSMC3 [HSA:5702] [KO:K03065]
(LAGNS) WSB2 [HSA:55884] [KO:K10342]
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