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Entry Name Description Category Pathway Gene
H00480 X-linked mental retardation X-linked mental retardation (XLMR) is an inherited condition that causes failure to develop cognitive abilities because of mutations in several genes on the X chromosome. XLMR is subdivided into syndromic ... Mental and behavioural disorder hsa04810 Regulation of actin cytoskeleton (MRX1/78) IQSEC2 [HSA:23096] [KO:K12495]
(MRX3) HCFC1 [HSA:3054] [KO:K14966]
(MRX9/44) FTSJ1 [HSA:24140] [KO:K14864]
(MRX12/35) THOC2 [HSA:57187] [KO:K12879]
(MRX19) RPS6KA3 [HSA:6197] [KO:K04373]
(MRX21/34) IL1RAPL1 [HSA:11141] [KO:K05170]
(MRX29s) ARX [HSA:170302] [KO:K09452]
(MRX30/47) PAK3 [HSA:5063] [KO:K05733]
(MRX41) GDI1 [HSA:2664] [KO:K17255]
(MRX46) ARHGEF6 [HSA:9459] [KO:K05729]
(MRX49/15) CLCN4 [HSA:1183] [KO:K05012]
(MRX58) TSPAN7 [HSA:7102] [KO:K06571]
(MRX61) RLIM [HSA:51132] [KO:K16271]
(MRX63) ACSL4 [HSA:2182] [KO:K01897]
(MRX72) RAB39B [HSA:116442] [KO:K07925]
(MRX90) DLG3 [HSA:1741] [KO:K21098]
(MRX91) ZDHHC15 [HSA:158866] [KO:K20028]
(MRX93) BRWD3 [HSA:254065] [KO:K11798]
(MRX96) SYP [HSA:6855]
(MRX97) ZNF711 [HSA:7552] [KO:K24376]
(MRX98) NEXMIF [HSA:340533]
(MRX99) USP9X [HSA:8239] [KO:K11840]
(MRX100) KIF4A [HSA:24137] [KO:K10395]
(MRX101) MID2 [HSA:11043] [KO:K10647]
(MRX102) DDX3X [HSA:1654] [KO:K11594]
(MRX103) KLHL15 [HSA:80311] [KO:K10452]
(MRX104) FRMPD4 [HSA:9758] [KO:K23956]
(MRX105) USP27X [HSA:389856] [KO:K11366]
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