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01 Mental Retardation, X-Linked [NCBI]

Gene


 Gene Link Information
Gain		 01
MRX80 [NCBI] 0.000373825
MRX84 [NCBI] 0.000373825
MRX77 [NCBI] 0.000373825
MRX78 [NCBI] 0.000373825
MRX81 [NCBI] 0.000373825
WTRS [NCBI] 0.000313087
ARX [NCBI] 0.000220193
FRAXA [NCBI] 0.000197818
OPHN1 [NCBI] 0.000122158
ATRX [NCBI] 0.000115144
SLC6A8 [NCBI] 9.37848e-05
MED12 [NCBI] 6.72687e-05
IL1RAPL1 [NCBI] 5.7851e-05
PHF8 [NCBI] 5.56084e-05
JARID1C [NCBI] 5.33471e-05
SLC16A2 [NCBI] 5.14011e-05
FTSJ1 [NCBI] 4.92892e-05
MECP2 [NCBI] 4.37168e-05
AP1S2 [NCBI] 3.77689e-05
PQBP1 [NCBI] 3.44219e-05
PAK3 [NCBI] 3.16545e-05
FMR1 [NCBI] 2.92976e-05
HSD17B10 [NCBI] 2.76552e-05
EHMT2 [NCBI] 2.33703e-05
CUL4B [NCBI] 2.27373e-05
TSPAN7 [NCBI] 2.09738e-05
JARID1A [NCBI] 2.09738e-05
ACSL4 [NCBI] 2.03464e-05
GDI1 [NCBI] 1.74377e-05
RPS6KA3 [NCBI] 1.66731e-05
AFF2 [NCBI] 1.58126e-05
UPF3B [NCBI] 1.49574e-05
FAM120C [NCBI] 1.49574e-05
ZCCHC12 [NCBI] 1.49574e-05
IPO13 [NCBI] 1.49574e-05
KIAA2022 [NCBI] 1.49574e-05
ZDHHC15 [NCBI] 1.49574e-05
ZNF674 [NCBI] 1.49574e-05
AGTR2 [NCBI] 1.47722e-05
NDP [NCBI] 1.4302e-05
UPF3A [NCBI] 1.25772e-05
TMEM47 [NCBI] 1.25772e-05
NXF5 [NCBI] 1.25772e-05
SHROOM4 [NCBI] 1.25772e-05
MAGT1 [NCBI] 1.25772e-05
BRWD3 [NCBI] 1.25772e-05
ARHGEF9 [NCBI] 1.25772e-05
P2RY8 [NCBI] 1.16789e-05
CDKL3 [NCBI] 1.16789e-05
ZDHHC9 [NCBI] 1.16789e-05
SLC9A6 [NCBI] 1.16789e-05
ZNF81 [NCBI] 1.16789e-05
ZNF41 [NCBI] 1.16789e-05
DCP2 [NCBI] 1.16789e-05
FREQ [NCBI] 1.10957e-05
WNK3 [NCBI] 1.10957e-05
VCX3A [NCBI] 1.10957e-05
IL1RAPL2 [NCBI] 1.06621e-05
CASK [NCBI] 1.06621e-05
PLP2 [NCBI] 1.03166e-05
DLG3 [NCBI] 1.03166e-05
SMS [NCBI] 1.03166e-05
JARID1D [NCBI] 1.03166e-05
PCDH19 [NCBI] 1.03166e-05
TUSC3 [NCBI] 1.00294e-05
HUWE1 [NCBI] 9.78352e-06
UBE2A [NCBI] 9.5686e-06
NLGN4X [NCBI] 9.37769e-06
VCX [NCBI] 9.37769e-06
PHF6 [NCBI] 9.37769e-06
GRIA3 [NCBI] 9.04992e-06
JARID1B [NCBI] 8.90694e-06
RPL10 [NCBI] 8.775e-06
SMARCA1 [NCBI] 8.65253e-06
REST [NCBI] 8.43113e-06
OFD1 [NCBI] 8.43113e-06
ATP6AP2 [NCBI] 8.23518e-06
RBBP7 [NCBI] 8.05943e-06
SOX3 [NCBI] 7.37993e-06
ALAS2 [NCBI] 7.16943e-06
ALS2 [NCBI] 7.02708e-06
L1CAM [NCBI] 6.24055e-06
GH1 [NCBI] 5.70648e-06
SHOX [NCBI] 4.99103e-06
ATP7A [NCBI] 4.5755e-06
DMD [NCBI] 4.36903e-06
BTK [NCBI] 3.19214e-06
AR [NCBI] 3.07137e-06
PML [NCBI] 2.84668e-06



OMIM


 OMIM Link Information
gain		 01
MRX78 [NCBI] 0.00159179
ARX [NCBI] 0.000388365
creatine deficiency syndrome, x-linked [NCBI] 0.000285002
OPHN1 [NCBI] 0.0002504
SLC6A8 [NCBI] 0.000225411
PQBP1 [NCBI] 0.000219689
siderius x-linked mental retardation syndrome [NCBI] 0.000215851
PHF8 [NCBI] 0.000211261
IL1RAPL1 [NCBI] 0.000192287
MRX59 [NCBI] 0.000192272
mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance [NCBI] 0.000192272
clark-baraitser syndrome [NCBI] 0.00018492
ATRX [NCBI] 0.000182715
CLS [NCBI] 0.00017416
RENS1 [NCBI] 0.00015641
ATRX [NCBI] 0.000129034
CUL4B [NCBI] 0.000128018
AP1S2 [NCBI] 0.000128018
MRX91 [NCBI] 0.000123215
JARID1C [NCBI] 0.000122132
FTSJ1 [NCBI] 0.000122132
AGTR2 [NCBI] 0.000117623
FACL4 [NCBI] 0.000110875
stocco dos santos x-linked mental retardation syndrome [NCBI] 0.00010075
MRX93 [NCBI] 0.00010075
MRX45 [NCBI] 0.00010075
mental retardation, x-linked, with brachydactyly and macroglossia [NCBI] 0.00010075
mental retardation, x-linked, with short stature, small testes, muscle wasting, and tremor [NCBI] 0.00010075
XMRE [NCBI] 0.00010075
MRXS10 [NCBI] 0.00010075
autism, x-linked, susceptibility to, 2 [NCBI] 0.00010075
MRXS14 [NCBI] 0.00010075
SLC16A2 [NCBI] 9.85428e-05
MRX63 [NCBI] 9.22761e-05
chromosome xp11.3 deletion syndrome [NCBI] 9.22761e-05
MRGH [NCBI] 9.22761e-05
simpson-golabi-behmel syndrome, type 2 [NCBI] 8.67758e-05
PRTS [NCBI] 8.67758e-05
roifman syndrome [NCBI] 8.67758e-05
ATP7A [NCBI] 7.7824e-05
ZDHHC9 [NCBI] 7.77002e-05
kiaa2022 [NCBI] 7.77002e-05
IPO13 [NCBI] 7.77002e-05
P2RY8 [NCBI] 7.77002e-05
SHROOM4 [NCBI] 7.77002e-05
FREQ [NCBI] 7.77002e-05
ZNF41 [NCBI] 7.77002e-05
ZDHHC15 [NCBI] 7.77002e-05
amme complex [NCBI] 7.67254e-05
MRX9 [NCBI] 7.44097e-05
lujan-fryns syndrome [NCBI] 7.44097e-05
chromosome 22q13.3 deletion syndrome [NCBI] 6.75057e-05
DCP2 [NCBI] 6.39235e-05
ZNF673 [NCBI] 6.39235e-05
DLG3 [NCBI] 6.39235e-05
BRWD3 [NCBI] 6.39235e-05
ZNF674 [NCBI] 6.39235e-05
BRWD2 [NCBI] 6.39235e-05
UPF3B [NCBI] 6.39235e-05
AHDS [NCBI] 6.07448e-05
BFLS [NCBI] 5.90062e-05
ZNF81 [NCBI] 5.8726e-05
ATP6AP2 [NCBI] 5.8726e-05
NLGN4 [NCBI] 5.8726e-05
NLGN3 [NCBI] 5.8726e-05
VCX3A [NCBI] 5.53521e-05
UBE2A [NCBI] 5.53521e-05
MRXHF1 [NCBI] 5.47049e-05
PHF6 [NCBI] 5.28443e-05
MED12 [NCBI] 5.28443e-05
OKS [NCBI] 5.23746e-05
AOF2 [NCBI] 5.08467e-05
TM4SF2 [NCBI] 5.08467e-05
immunodeficiency-centromeric instability-facial anomalies syndrome [NCBI] 5.03452e-05
ARHGEF6 [NCBI] 4.91861e-05
cardiofaciocutaneous syndrome [NCBI] 4.73251e-05
GDI1 [NCBI] 4.65233e-05
HSD17B10 [NCBI] 4.65233e-05
SOX3 [NCBI] 4.65233e-05
CXORF5 [NCBI] 4.54204e-05
costello syndrome [NCBI] 4.29165e-05
RSTS [NCBI] 4.07216e-05
FRAXE [NCBI] 3.83081e-05
REST [NCBI] 3.78148e-05
RPS6KA3 [NCBI] 3.64688e-05
menkes disease [NCBI] 3.53925e-05
NS1 [NCBI] 3.35402e-05
DMD [NCBI] 2.38201e-05
ABCG2 [NCBI] 2.25207e-05
MECP2 [NCBI] 1.9997e-05
RTT [NCBI] 1.94727e-05
CF [NCBI] 1.79274e-05



Database Center for Life Science