ASD

GO:0030900 forebrain development (225)

GeneInput weightStandardRank
GNAO1--3
ATRX--124
SLIT1--33
GRIN2A0.25156
PLCB1--161
ERBB40.25164
SLC1A2--71
SOX2--1125
CNTNAP21.01134
NEUROD1--1136
FGFR2--1165
GRIN1--167
SSTR2--185
PAFAH1B10.251208
ASCL1--229
SLC8A2--232
NFIB--271
RARB0.251325
NF10.251333
PAX60.251355
LHX2--362
NEUROD6--385
TOP2B--389
MYH10--403
CDK5R1--406
SALL1--408
RELN0.51436
CNTN2--438
NPY0.251456
HPRT1--1481
FOXG1--483
GNAQ--490
FABP70.251563
SLIT2--582
NR4A3--1594
GRIN2B1.01599
PCSK1--604
POU3F2--653
DRD10.251662
CHRD--697
NR2E10.251699
FEZF20.251712
NR4A20.251713
LRP20.251745
SMARCA4--751
YWHAE--772
LRP6--778
DICER1--1834
VLDLR0.251837
PGAP1--865
RFX4--924
CREB1--991
RAC1--1087
PRKG1--1091
DLC1--1105
WNT2B--1126
BCL11B--1127
ID4--1171
BCAN--1186
NDEL10.2511194
NR2F1--1220
ROBO2--11224
DLX20.2511235
FYN--1284
OTX2--11295
SLC8A1--1339
HDAC2--1413
ISL1--1441
HTR5A0.2511507
AKAP5--1517
SALL3--1561
GSK3B--1592
FGFR3--11648
TYRO3--1663
NR0B1--11715
ID2--1719
LEF1--1731
SIX3--11742
RTN4--1776
NCOR1--1807
EMX1--1823
TSC10.2511844
ROBO1--1888
LHX1--1926
APP--1991
SOX3--2042
BMPR1A--2059
DRD20.2512071
DPYSL2--2131
LRP8--2215
SRC--2241
GHRHR--2312
NEUROG2--2345
MSX1--12365
DLX10.2512366
NKX2-1--2488
MAPK8IP3--2496
WNT8B--2506
FGFR1--2550
LHX5--2646
ZEB1--12672
GATA2--12710
TNR--2784
EGFR--12811
WNT5A--2870
GSX1--2967
LHX6--2989
LHX8--3040
CDK50.2513113
AVPR1A0.513141
CYP17A10.2513171
WNT1--3263
MAS1--3300
CYP19A10.2513314
SLC6A40.2513328
NOTCH1--13360
RAX--13411
AGTPBP1--3437
ALDH1A2--3466
CDON--3482
PTPRS--3537
PCM1--13562
SLC8A3--3637
BMP2--13686
SRD5A10.2513730
OGDH--3773
EXT10.2513907
HES5--4001
OTX1--4110
FOXB1--4202
FOXP20.514225
SKI--4231
FGF10--14373
MECOM--4397
DIXDC1--4469
OXTR0.514494
OTP--4497
AVPR2--14537
DRAXIN--4545
CYP11A10.2514559
GHRH--4568
ZEB2--4607
NR2F2--4609
WNT3A--4844
BMP4--15180
PLXNA4--5187
ETS1--5230
SLC6A30.2515276
ATP7A--15491
LMX1A--5502
HES10.2515662
GLI2--15731
NDST1--5799
SMO0.2515864
CTNNB10.2516229
GSX2--6242
WNT7A--6375
PRTFDC1--6437
TH0.2516482
DKK1--6892
CXCL12--7204
GDF7--7494
CCKAR--7616
NOG--17650
WNT7B--7693
HSD17B30.2517714
CX3CR1--7884
GSC--8075
NUMBL--8142
AHSG--8418
PEX5--18514
KDM2B--8663
UQCRQ--8688
GLI3--19032
ATOH1--9258
TAL2--9456
FGF2--9627
DUOX2--19797
NUMB--9921
HOOK3--10195
BBS4--110693
AXIN1--110905
EOMES--11394
FEZF10.25111491
GNG12--11929
SSTR3--12043
FRS2--12610
RYK--12768
IFT88--12821
MKKS--112900
TACC3--13022
LRRK2--113335
E2F1--13572
BBS2--114317
TBX19--14813
ALDH1A3--15783
SHH--115942
TP73--15964
KDM1A--15967
CEP120--18769
RPGRIP1L--19545
PSEN1--20241
CHRNB20.25120277
EFNA2--20349
HESX1--20697
ANXA3--20797
AQP1--21019
NKX2-6--121164
ARX0.25121412
PSEN2--21431
AXL--21695
WNT4--21840
RAB3GAP1--22229
MDK--22267
NOTCH3--22751
WDR62--22764
KAT2A--22874
PITX10.25123078
HTRA2--123310
CDH1--123441
UCHL5--23734
ATG7--23783
PEX13--124706
TWSG1--25171
ASPM--125468

Network

GO:0030900

Network
Enrichment
NameDescriptionExternal IDs
GNAO1guanine nucleotide binding protein (G protein), alpha activating activity polypeptide O Entrez:2775  HPRD: 00757  HGNC: 4389  Ensembl: ENSG00000087258 
ATRXalpha thalassemia/mental retardation syndrome X-linked Entrez:546  HGNC: 886  HPRD: 02069  Ensembl: ENSG00000085224 
SLIT1slit homolog 1 (Drosophila) Entrez:6585  Ensembl: ENSG00000187122  HGNC: 11085  HPRD: 04773 
GRIN2Aglutamate receptor, ionotropic, N-methyl D-aspartate 2A Entrez:2903  HGNC: 4585  Ensembl: ENSG00000183454  HPRD: 00698 
PLCB1phospholipase C, beta 1 (phosphoinositide-specific) Entrez:23236  HGNC: 15917  HPRD: 06177  Ensembl: ENSG00000182621 
GenesetTypeFreq. (Network vs Genome)P-Value (FDR Corrected)Genes
GeneDescriptionAvg. edge score to queryRankIn genesetIn query
GNAO1guanine nucleotide binding protein (G protein), alpha activating activity polypeptide O
ATRXalpha thalassemia/mental retardation syndrome X-linked
SLIT1slit homolog 1 (Drosophila)
GRIN2Aglutamate receptor, ionotropic, N-methyl D-aspartate 2A
PLCB1phospholipase C, beta 1 (phosphoinositide-specific)
Query geneGeneGene descriptionEdge score
GNAO1GNAO1guanine nucleotide binding protein (G protein), alpha activating activity polypeptide O
ATRXATRXalpha thalassemia/mental retardation syndrome X-linked
SLIT1SLIT1slit homolog 1 (Drosophila)
GRIN2AGRIN2Aglutamate receptor, ionotropic, N-methyl D-aspartate 2A
PLCB1PLCB1phospholipase C, beta 1 (phosphoinositide-specific)

Troyanskaya Laboratory - Princeton University