Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Myelin P0 Protein [NCBI]


Gene


Gene Link Information
Gain
01
MPZ [NCBI] 0.000269301
PMP22 [NCBI] 0.00017393
GJB1 [NCBI] 7.73832e-05
MS [NCBI] 5.5892e-05
MBP [NCBI] 3.90126e-05
EGR2 [NCBI] 1.22942e-05
GDAP1 [NCBI] 7.09514e-06
MAG [NCBI] 6.4257e-06
LITAF [NCBI] 5.31959e-06
NEFL [NCBI] 4.90529e-06
GFAP [NCBI] 4.34922e-06
MAD2L1BP [NCBI] 3.62003e-06
MTMR2 [NCBI] 3.35207e-06
KIF1B [NCBI] 3.26272e-06
POU3F1 [NCBI] 3.19821e-06
MFN2 [NCBI] 2.96551e-06
MOG [NCBI] 2.82118e-06
SOX10 [NCBI] 2.65772e-06
SIGLEC1 [NCBI] 2.60326e-06
NEFM [NCBI] 2.27728e-06
RAB7A [NCBI] 2.27299e-06
NEFH [NCBI] 1.88201e-06
CDRT1 [NCBI] 1.72913e-06
PRB4 [NCBI] 1.72913e-06
MYRIP [NCBI] 1.72913e-06
MPZL1 [NCBI] 1.69217e-06
SH3TC2 [NCBI] 1.69217e-06
PLLP [NCBI] 1.67545e-06
SBF2 [NCBI] 1.63078e-06
CNTNAP1 [NCBI] 1.63078e-06
PRX [NCBI] 1.60467e-06
GAN [NCBI] 1.59252e-06
MAL [NCBI] 1.58089e-06
UBE4B [NCBI] 1.56975e-06
PRPH [NCBI] 1.53887e-06
RAG1 [NCBI] 1.53804e-06
CNTNAP2 [NCBI] 1.47064e-06
QKI [NCBI] 1.46322e-06
MYT1 [NCBI] 1.456e-06
DNM2 [NCBI] 1.3513e-06
HSPB8 [NCBI] 1.34185e-06
NDRG1 [NCBI] 1.33725e-06
FXR1 [NCBI] 1.32828e-06
NCOA1 [NCBI] 1.1536e-06
GNB2L1 [NCBI] 1.11339e-06
CNTN1 [NCBI] 1.08903e-06
KLRB1 [NCBI] 1.07508e-06
CTNNB1 [NCBI] 1.02301e-06
PVR [NCBI] 9.76959e-07
AR [NCBI] 9.29208e-07
APOE [NCBI] 8.81358e-07
LMNA [NCBI] 8.73868e-07
ERG [NCBI] 7.9091e-07
HSPB1 [NCBI] 7.61223e-07
CLU [NCBI] 7.59192e-07
TNF [NCBI] 6.99911e-07
CAV1 [NCBI] 6.6726e-07
IFNGR1 [NCBI] 6.1648e-07
PRKCA [NCBI] 6.07183e-07
PAX6 [NCBI] 5.92167e-07
TF [NCBI] 5.80483e-07
NGF [NCBI] 1.53725e-07
EGF [NCBI] 5.60483e-08




OMIM


OMIM Link Information
gain
01
MPZ [NCBI] 0.0027687
hypertrophic neuropathy of dejerine-sottas [NCBI] 0.00260041
neuropathy, congenital hypomyelinating [NCBI] 0.00110724
charcot-marie-tooth disease, axonal, type 2j [NCBI] 0.00100401
CMT1A [NCBI] 0.000835148
PMP22 [NCBI] 0.000760753
MAG [NCBI] 0.000715124
charcot-marie-tooth disease, axonal, type 2i [NCBI] 0.000499502
CMT1B [NCBI] 0.00040576
MBP [NCBI] 0.000359947
GJB1 [NCBI] 0.000299343
roussy-levy hereditary areflexic dystasia [NCBI] 0.000165967
charcot-marie-tooth disease, dominant intermediate d [NCBI] 0.000165967
adie pupil [NCBI] 0.000134391
charcot-marie-tooth disease and deafness [NCBI] 0.000114755
CMT4B1 [NCBI] 0.000109013
charcot-marie-tooth disease, axonal, type 2b1 [NCBI] 0.00010444
EGR2 [NCBI] 7.11379e-05
KIF1B [NCBI] 2.53371e-05
POU3F1 [NCBI] 2.30112e-05
MYT1 [NCBI] 2.18849e-05
DNM2 [NCBI] 2.14006e-05
GDAP1 [NCBI] 2.0957e-05
EGF [NCBI] 2.07573e-05
NTRK3 [NCBI] 2.01682e-05
NTF3 [NCBI] 1.94823e-05
NEFL [NCBI] 1.8597e-05
DHH [NCBI] 1.62361e-05
GFAP [NCBI] 1.30943e-05
NRG1 [NCBI] 9.46155e-06
NGFB [NCBI] 7.81759e-06
NGFR [NCBI] 7.57721e-06
TNF [NCBI] 6.8421e-06
FMR1 [NCBI] 6.35082e-06
TF [NCBI] 7.72666e-07
APOE [NCBI] 3.85697e-07
AR [NCBI] 2.11033e-07




Database Center for Life Science