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01 Nervous System Malformations [NCBI]


Gene


Gene Link Information
Gain
01
BPP [NCBI] 0.000415947
SPG32 [NCBI] 0.000415947
RELN [NCBI] 0.000192372
PAFAH1B1 [NCBI] 0.000175824
AIS [NCBI] 0.000140171
PAX6 [NCBI] 7.41857e-05
DCX [NCBI] 6.6318e-05
NTN1 [NCBI] 4.4858e-05
GFAP [NCBI] 2.91995e-05
OPHN1 [NCBI] 2.91681e-05
LRP8 [NCBI] 2.83253e-05
EN2 [NCBI] 2.83253e-05
DCLK1 [NCBI] 2.32242e-05
GPR56 [NCBI] 2.02004e-05
HOXA1 [NCBI] 1.82784e-05
CNTN2 [NCBI] 1.74165e-05
VLDLR [NCBI] 1.74165e-05
FLNA [NCBI] 1.55918e-05
DLX3 [NCBI] 1.52388e-05
DCLK2 [NCBI] 1.48846e-05
FOXP2 [NCBI] 1.47991e-05
L1CAM [NCBI] 1.47407e-05
SNAP29 [NCBI] 1.25043e-05
KIAA1279 [NCBI] 1.16061e-05
NFASC [NCBI] 1.10229e-05
MAP2 [NCBI] 1.09451e-05
NEFL [NCBI] 1.08708e-05
ARFGEF2 [NCBI] 1.05893e-05
GRM5 [NCBI] 1.05556e-05
NFIA [NCBI] 1.02439e-05
THEM4 [NCBI] 1.02439e-05
RCAN2 [NCBI] 9.95664e-06
ARHGAP26 [NCBI] 9.71078e-06
SYNM [NCBI] 9.71078e-06
ROBO3 [NCBI] 9.71078e-06
SLIT1 [NCBI] 9.13326e-06
RPL14 [NCBI] 8.97723e-06
POMT1 [NCBI] 8.83427e-06
ATR [NCBI] 8.67323e-06
NKX2-1 [NCBI] 8.60803e-06
SLC12A6 [NCBI] 8.57987e-06
POU4F2 [NCBI] 8.46561e-06
SPG11 [NCBI] 8.46561e-06
PRPH [NCBI] 8.46561e-06
SV2A [NCBI] 8.46561e-06
CDC45L [NCBI] 8.35851e-06
NIPA1 [NCBI] 8.35851e-06
LARGE [NCBI] 8.16258e-06
EIF2B5 [NCBI] 8.16258e-06
AHI1 [NCBI] 7.90535e-06
ANK2 [NCBI] 7.90535e-06
OLIG1 [NCBI] 7.75317e-06
POU4F1 [NCBI] 7.75317e-06
CNTN1 [NCBI] 7.6819e-06
MBP [NCBI] 7.61595e-06
HS3ST5 [NCBI] 7.61349e-06
FGFR3 [NCBI] 7.60993e-06
GRID2 [NCBI] 7.54772e-06
NCAN [NCBI] 7.4844e-06
MCPH1 [NCBI] 7.09702e-06
ACTB [NCBI] 7.00083e-06
NCK1 [NCBI] 6.95471e-06
ATL1 [NCBI] 6.90981e-06
HESX1 [NCBI] 6.90981e-06
OLIG2 [NCBI] 6.66287e-06
PLA2G7 [NCBI] 6.44743e-06
LGI1 [NCBI] 6.44743e-06
CDC42 [NCBI] 6.34921e-06
FKRP [NCBI] 6.31771e-06
ARX [NCBI] 6.08486e-06
FKTN [NCBI] 6.00524e-06
PITX3 [NCBI] 5.92922e-06
LAMA1 [NCBI] 5.8565e-06
HES1 [NCBI] 5.83294e-06
NEFM [NCBI] 5.71989e-06
MCM2 [NCBI] 5.67673e-06
MARCKS [NCBI] 5.43885e-06
WNT1 [NCBI] 5.40231e-06
NID1 [NCBI] 5.12045e-06
PAX2 [NCBI] 4.96073e-06
EIF4EBP1 [NCBI] 4.93328e-06
RHOA [NCBI] 4.90629e-06
MUSK [NCBI] 4.86661e-06
ADCYAP1 [NCBI] 4.74086e-06
CDC25A [NCBI] 4.71683e-06
SOX9 [NCBI] 4.68143e-06
ERCC5 [NCBI] 4.64679e-06
RAC1 [NCBI] 4.62409e-06
TH [NCBI] 4.60015e-06
ATXN1 [NCBI] 4.2263e-06
CDK5 [NCBI] 4.11561e-06
BMP4 [NCBI] 3.92213e-06
FOXO1 [NCBI] 3.80964e-06
DAG1 [NCBI] 3.78272e-06
NEFH [NCBI] 3.63631e-06
NOTCH1 [NCBI] 3.57669e-06
ERBB4 [NCBI] 3.39477e-06
CTNNB1 [NCBI] 3.34589e-06
PROM1 [NCBI] 3.29413e-06
SHH [NCBI] 3.29413e-06
AFP [NCBI] 2.71286e-06
CHEK1 [NCBI] 2.61338e-06
FMR1 [NCBI] 1.89944e-06
SOD1 [NCBI] 1.44258e-06
BDNF [NCBI] 1.34753e-06
STAT3 [NCBI] 1.33171e-06
PTEN [NCBI] 1.07563e-06
AR [NCBI] 6.04552e-07
NGF [NCBI] 5.50179e-07
EGF [NCBI] 6.61536e-08




OMIM


OMIM Link Information
gain
01
SPG32 [NCBI] 0.00106493
NLS [NCBI] 0.00104072
polymicrogyria, unilateral [NCBI] 0.000847142
megalencephaly [NCBI] 0.000765046
lateral meningocele syndrome [NCBI] 0.000672238
centralopathic epilepsy [NCBI] 0.000512699
VUR1 [NCBI] 0.000408926
chiari malformation type i [NCBI] 0.000402807
MBS [NCBI] 0.00036587
autism [NCBI] 0.000332646
polymicrogyria, bilateral frontoparietal [NCBI] 0.000303363
LIS1 [NCBI] 0.00027794
PAFAH1B1 [NCBI] 0.000206921
FCDT [NCBI] 0.000173919
BPP [NCBI] 0.000165743
megalencephaly-cutis marmorata telangiectatica congenita [NCBI] 0.000162322
heterotopia, periventricular, x-linked dominant [NCBI] 0.000147098
autonomic control, congenital failure of [NCBI] 0.000125756
cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [NCBI] 0.000123215
LRP8 [NCBI] 0.00011598
IS1 [NCBI] 0.000107147
GFAP [NCBI] 0.000102972
VUR2 [NCBI] 0.00010075
dystonia, juvenile-onset [NCBI] 0.00010075
TD1 [NCBI] 9.62042e-05
lissencephaly type iii and bone dysplasia [NCBI] 9.22761e-05
VLDLR [NCBI] 9.15781e-05
mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance [NCBI] 8.26879e-05
macrocephaly/autism syndrome [NCBI] 7.94318e-05
SV2A [NCBI] 7.68849e-05
SLC17A6 [NCBI] 7.68849e-05
lady bird late, drosophila, homolog of, 1 [NCBI] 7.68849e-05
KIAA1279 [NCBI] 7.68849e-05
DCAMKL1 [NCBI] 7.68849e-05
SNAP29 [NCBI] 7.68849e-05
goldberg-shprintzen megacolon syndrome [NCBI] 7.67254e-05
HGPPS [NCBI] 7.67254e-05
sulfocysteinuria [NCBI] 7.67254e-05
TS [NCBI] 7.45909e-05
rokitansky-kuster-hauser syndrome [NCBI] 7.44097e-05
corpus callosum, agenesis of [NCBI] 7.2386e-05
LISX1 [NCBI] 7.05892e-05
oculocerebrocutaneous syndrome [NCBI] 6.75057e-05
hydrocephalus [NCBI] 6.61613e-05
HHS [NCBI] 6.49211e-05
TRAK1 [NCBI] 6.31085e-05
CDH8 [NCBI] 6.31085e-05
ATSV [NCBI] 5.79114e-05
GNAO1 [NCBI] 5.79114e-05
NFIA [NCBI] 5.79114e-05
ROBO3 [NCBI] 5.79114e-05
VWM [NCBI] 5.47049e-05
MLC [NCBI] 5.47049e-05
CDH11 [NCBI] 5.45379e-05
LIMK1 [NCBI] 5.45379e-05
ACTB [NCBI] 5.20304e-05
CDH2 [NCBI] 5.00331e-05
ODDD [NCBI] 4.94212e-05
MEB [NCBI] 4.85487e-05
PPARBP [NCBI] 4.83729e-05
walker-warburg syndrome [NCBI] 4.73251e-05
cardiofaciocutaneous syndrome [NCBI] 4.73251e-05
PRPH [NCBI] 4.69523e-05
OPHN1 [NCBI] 4.57107e-05
MCPH1 [NCBI] 4.57107e-05
CASP3 [NCBI] 4.57107e-05
AN2 [NCBI] 4.3828e-05
SEMA3A [NCBI] 4.36168e-05
DCX [NCBI] 4.27162e-05
GATA3 [NCBI] 4.27162e-05
POMT1 [NCBI] 4.18911e-05
RELN [NCBI] 4.18911e-05
EIF2B5 [NCBI] 4.18911e-05
LKS [NCBI] 4.09793e-05
MAPK3 [NCBI] 3.97648e-05
ERCC5 [NCBI] 3.44799e-05
GCDH [NCBI] 3.4116e-05
SHH [NCBI] 3.40442e-05
FLNA [NCBI] 3.13401e-05
L1CAM [NCBI] 3.10757e-05
IP [NCBI] 2.83989e-05
PAX6 [NCBI] 2.67457e-05
BCNS [NCBI] 2.50665e-05
FGFR1 [NCBI] 2.30899e-05
WBS [NCBI] 2.28265e-05
CDK5 [NCBI] 2.11771e-05
MBP [NCBI] 2.10663e-05
LRP1 [NCBI] 1.97522e-05
ADCYAP1 [NCBI] 1.89382e-05
PTEN [NCBI] 1.87979e-05
FGFR2 [NCBI] 1.87979e-05
MAG [NCBI] 1.49351e-05
phenylketonuria [NCBI] 1.4094e-05
FGFR3 [NCBI] 1.39358e-05
RB1 [NCBI] 1.39358e-05
ACE [NCBI] 1.22796e-05
TH [NCBI] 1.10399e-05
FTD [NCBI] 8.00622e-06
AFP [NCBI] 3.63857e-06
EGF [NCBI] 2.55378e-06
BDNF [NCBI] 1.90924e-06
AR [NCBI] 2.55121e-07
NGFB [NCBI] 8.96624e-10




Database Center for Life Science