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{"sheet":"Sheet1","index":0,"n_rows":91,"n_cols":4,"rows_kept":91,"cut":false,"hidden":false,"merged":[]}
[null,"abnormal nervous system physiology; MP:0003633"]
[null,"Entrez Gene ID","Gene Symbol","Gene Name"]
[1,6812,"STXBP1","syntaxin binding protein 1"]
[2,1641,"DCX","doublecortin"]
[3,6323,"SCN1A","sodium channel, voltage-gated, type I, alpha subunit"]
[4,3000,"GUCY2D","guanylate cyclase 2D, membrane (retina-specific)"]
[5,8831,"SYNGAP1","synaptic Ras GTPase activating protein 1"]
[6,8573,"CASK","calcium/calmodulin-dependent serine protein kinase (MAGUK family)"]
[7,5728,"PTEN","phosphatase and tensin homolog"]
[8,775,"CACNA1C","calcium channel, voltage-dependent, L type, alpha 1C subunit"]
[9,10479,"SLC9A6","solute carrier family 9 (sodium/hydrogen exchanger), member 6"]
[10,1387,"CREBBP","CREB binding protein"]
[11,10743,"RAI1","retinoic acid induced 1"]
[12,7915,"ALDH5A1","aldehyde dehydrogenase 5 family, member A1"]
[13,4669,"NAGLU","N-acetylglucosaminidase, alpha"]
[14,3767,"KCNJ11","potassium inwardly-rectifying channel, subfamily J, member 11"]
[15,4204,"MECP2","methyl CpG binding protein 2 (Rett syndrome)"]
[16,2263,"FGFR2","fibroblast growth factor receptor 2"]
[17,4693,"NDP","Norrie disease (pseudoglioma)"]
[18,7337,"UBE3A","ubiquitin protein ligase E3A"]
[19,6853,"SYN1","synapsin I"]
[20,54413,"NLGN3","neuroligin 3"]
[21,4983,"OPHN1","oligophrenin 1"]
[22,6899,"TBX1","T-box 1"]
[23,11141,"IL1RAPL1","interleukin 1 receptor accessory protein-like 1"]
[24,2290,"FOXG1","forkhead box G1"]
[25,8492,"PRSS12","protease, serine, 12 (neurotrypsin, motopsin)"]
[26,55636,"CHD7","chromodomain helicase DNA binding protein 7"]
[27,7531,"YWHAE","tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide"]
[28,5009,"OTC","ornithine carbamoyltransferase"]
[29,673,"BRAF","v-raf murine sarcoma viral oncogene homolog B1"]
[30,2334,"AFF2","AF4/FMR2 family, member 2"]
[31,2332,"FMR1","fragile X mental retardation 1"]
[32,5053,"PAH","phenylalanine hydroxylase"]
[33,9378,"NRXN1","neurexin 1"]
[34,5048,"PAFAH1B1","platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)"]
[35,7248,"TSC1","tuberous sclerosis 1"]
[36,7249,"TSC2","tuberous sclerosis 2"]
[37,186,"AGTR2","angiotensin II receptor, type 2"]
[38,170302,"ARX","aristaless related homeobox"]
[39,6121,"RPE65","retinal pigment epithelium-specific protein 65kDa"]
[40,5781,"PTPN11","protein tyrosine phosphatase, non-receptor type 11"]
[41,1717,"DHCR7","7-dehydrocholesterol reductase"]
[42,3897,"L1CAM","L1 cell adhesion molecule"]
[43,54806,"AHI1","Abelson helper integration site 1"]
[44,3845,"KRAS","v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog"]
[45,2892,"GRIA3","glutamate receptor, ionotrophic, AMPA 3"]
[46,2904,"GRIN2B","glutamate receptor, ionotropic, N-methyl D-aspartate 2B"]
[null,"abnormal synaptic transmission; MP:0003635"]
[null,"Entrez Gene ID","Gene Symbol","Gene Name"]
[1,6812,"STXBP1","syntaxin binding protein 1"]
[2,1641,"DCX","doublecortin"]
[3,6323,"SCN1A","sodium channel, voltage-gated, type I, alpha subunit"]
[4,8831,"SYNGAP1","synaptic Ras GTPase activating protein 1"]
[5,8573,"CASK","calcium/calmodulin-dependent serine protein kinase (MAGUK family)"]
[6,775,"CACNA1C","calcium channel, voltage-dependent, L type, alpha 1C subunit"]
[7,4204,"MECP2","methyl CpG binding protein 2 (Rett syndrome)"]
[8,7337,"UBE3A","ubiquitin protein ligase E3A"]
[9,6853,"SYN1","synapsin I"]
[10,54413,"NLGN3","neuroligin 3"]
[11,4983,"OPHN1","oligophrenin 1"]
[12,6899,"TBX1","T-box 1"]
[13,11141,"IL1RAPL1","interleukin 1 receptor accessory protein-like 1"]
[14,2334,"AFF2","AF4/FMR2 family, member 2"]
[15,2332,"FMR1","fragile X mental retardation 1"]
[16,9378,"NRXN1","neurexin 1"]
[17,7248,"TSC1","tuberous sclerosis 1"]
[18,7249,"TSC2","tuberous sclerosis 2"]
[19,1717,"DHCR7","7-dehydrocholesterol reductase"]
[20,2892,"GRIA3","glutamate receptor, ionotrophic, AMPA 3"]
[21,2904,"GRIN2B","glutamate receptor, ionotropic, N-methyl D-aspartate 2B"]
[null,"abnormal CNS synaptic transmission; MP:0002206"]
[null,"Entrez Gene ID","Gene Symbol","Gene Name"]
[1,1641,"DCX","doublecortin"]
[2,6323,"SCN1A","sodium channel, voltage-gated, type I, alpha subunit"]
[3,8831,"SYNGAP1","synaptic Ras GTPase activating protein 1"]
[4,775,"CACNA1C","calcium channel, voltage-dependent, L type, alpha 1C subunit"]
[5,4204,"MECP2","methyl CpG binding protein 2 (Rett syndrome)"]
[6,7337,"UBE3A","ubiquitin protein ligase E3A"]
[7,6853,"SYN1","synapsin I"]
[8,54413,"NLGN3","neuroligin 3"]
[9,4983,"OPHN1","oligophrenin 1"]
[10,6899,"TBX1","T-box 1"]
[11,11141,"IL1RAPL1","interleukin 1 receptor accessory protein-like 1"]
[12,2334,"AFF2","AF4/FMR2 family, member 2"]
[13,2332,"FMR1","fragile X mental retardation 1"]
[14,7248,"TSC1","tuberous sclerosis 1"]
[15,7249,"TSC2","tuberous sclerosis 2"]
[16,1717,"DHCR7","7-dehydrocholesterol reductase"]
[17,2892,"GRIA3","glutamate receptor, ionotrophic, AMPA 3"]
[18,2904,"GRIN2B","glutamate receptor, ionotropic, N-methyl D-aspartate 2B"]