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MeSH keywords -> Related genes, diseases (OMIM)


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01 Lip [NCBI]

Gene


 Gene Link Information
Gain		 01
GSM1 [NCBI] 0.000453044
VWS2 [NCBI] 0.000453044
GER [NCBI] 9.03629e-05
IRF6 [NCBI] 8.58206e-05
MS [NCBI] 3.15998e-05
MUC7 [NCBI] 1.92605e-05
RET [NCBI] 9.09332e-06
TROVE2 [NCBI] 8.83837e-06
CAMK1G [NCBI] 8.16956e-06
PPP1R14C [NCBI] 7.54735e-06
G0S2 [NCBI] 7.54735e-06
IGJ [NCBI] 6.39673e-06
SPRR1B [NCBI] 6.39673e-06
CST4 [NCBI] 6.067e-06
PSCA [NCBI] 5.59905e-06
DSC2 [NCBI] 5.55603e-06
NEK2 [NCBI] 5.45596e-06
HPRT1 [NCBI] 5.4371e-06
DMBT1 [NCBI] 5.07969e-06
HSD11B1 [NCBI] 4.79729e-06
AQP1 [NCBI] 4.6015e-06
APOD [NCBI] 4.14883e-06
DLX3 [NCBI] 4.01053e-06
TNFSF13B [NCBI] 3.88531e-06
CD83 [NCBI] 3.29805e-06
LAMB3 [NCBI] 3.25383e-06
XRCC5 [NCBI] 3.08601e-06
TGFBR1 [NCBI] 2.99518e-06
TF [NCBI] 2.99361e-06
CD38 [NCBI] 2.53487e-06
PTEN [NCBI] 2.47093e-06
CD68 [NCBI] 2.18177e-06
STAT3 [NCBI] 1.94873e-06
BAX [NCBI] 1.63684e-06
FASLG [NCBI] 1.54279e-06
BDNF [NCBI] 1.53254e-06
VIP [NCBI] 1.45649e-06
GFAP [NCBI] 1.37443e-06
ACHE [NCBI] 1.34047e-06
CDKN1A [NCBI] 1.24406e-06
PRL [NCBI] 1.17725e-06
NGF [NCBI] 8.94343e-07



OMIM


 OMIM Link Information
gain		 01
VWS [NCBI] 0.00411976
kabuki syndrome [NCBI] 0.00247344
lip, median nodule of upper [NCBI] 0.00133829
van der woude syndrome 2 [NCBI] 0.00133829
sclerotylosis [NCBI] 0.000911032
van der woude syndrome modifier [NCBI] 0.000911032
branchiootic syndrome 2 [NCBI] 0.000835362
hypertelorism, teebi type [NCBI] 0.000835362
acromegaloid facial appearance syndrome [NCBI] 0.000779239
GSM1 [NCBI] 0.000734627
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging [NCBI] 0.000638468
PPS [NCBI] 0.00060066
facial ectodermal dysplasia [NCBI] 0.000592139
OFC1 [NCBI] 0.000521929
cayler cardiofacial syndrome [NCBI] 0.00048141
LNS [NCBI] 0.000464942
coffin-siris syndrome [NCBI] 0.000427822
CPI [NCBI] 0.000376675
blepharochalasis and double lip [NCBI] 0.000369487
focal epithelial hyperplasia, oral [NCBI] 0.000291015
DA2A [NCBI] 0.000288928
focal epithelial hyperplasia of the oral mucosa [NCBI] 0.000184555
lip prints [NCBI] 0.000184555
ichthyosis with alopecia, eclabion, ectropion, and mental retardation [NCBI] 0.000184555
ackerman syndrome [NCBI] 0.000184555
commissural lip pits [NCBI] 0.000184555
craniorhiny [NCBI] 0.000145319
tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities [NCBI] 0.000145319
kniest-like dysplasia with pursed lips and ectopia lentis [NCBI] 0.000130536
oroacral syndrome, verloes-koulischer type [NCBI] 0.000120951
aglossia-adactylia [NCBI] 0.00010817
weaver syndrome [NCBI] 8.30309e-05
donohue syndrome [NCBI] 7.74685e-05
SMMCI [NCBI] 7.43097e-05
EVC [NCBI] 6.55084e-05
SJS1 [NCBI] 6.2482e-05
HOXA2 [NCBI] 5.44279e-05
IRF6 [NCBI] 4.75073e-05
DSC2 [NCBI] 4.33962e-05
HSD11B1 [NCBI] 4.07978e-05
CDLS1 [NCBI] 4.04506e-05
CF [NCBI] 3.96784e-05
SLE [NCBI] 3.82859e-05
RET [NCBI] 3.12304e-05
AQP1 [NCBI] 2.9329e-05
HPRT1 [NCBI] 2.81204e-05
SLC18A3 [NCBI] 2.30531e-05
RA [NCBI] 2.23226e-05
WBS [NCBI] 2.18077e-05
TF [NCBI] 1.54476e-05
TNFSF6 [NCBI] 9.97106e-06
BDNF [NCBI] 5.30956e-06
VIP [NCBI] 4.75624e-06
GFAP [NCBI] 4.28329e-06
ACHE [NCBI] 4.094e-06
PRL [NCBI] 3.14441e-06
NGFB [NCBI] 1.65978e-06
MG [NCBI] 8.218e-07
VEGF [NCBI] 6.80153e-07



Database Center for Life Science