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01 Penis [NCBI]

Gene


 Gene Link Information
Gain		 01
FSHMD1A [NCBI] 0.000304122
GUCY1B2 [NCBI] 0.000285008
PDE5A [NCBI] 0.000237193
MS [NCBI] 0.000132163
VUR [NCBI] 9.82178e-05
AR [NCBI] 7.71101e-05
VIP [NCBI] 3.36651e-05
NOS3 [NCBI] 3.11349e-05
NPY [NCBI] 2.928e-05
SRD5A2 [NCBI] 2.37145e-05
NOS1 [NCBI] 1.6399e-05
HOXA13 [NCBI] 1.39361e-05
FGF8 [NCBI] 1.20116e-05
AHRR [NCBI] 1.13538e-05
TGFB1 [NCBI] 1.08896e-05
OXTR [NCBI] 9.52152e-06
NOS2 [NCBI] 9.45725e-06
PDE3A [NCBI] 9.07615e-06
VEGFA [NCBI] 8.40101e-06
TH [NCBI] 8.32111e-06
LHCGR [NCBI] 8.29475e-06
NR5A1 [NCBI] 8.26803e-06
MAS1 [NCBI] 8.21564e-06
SLC18A3 [NCBI] 8.11484e-06
NGF [NCBI] 8.01359e-06
PRL [NCBI] 7.80377e-06
BMP4 [NCBI] 7.66032e-06
ESR1 [NCBI] 6.95424e-06
MSTN [NCBI] 6.404e-06
AMH [NCBI] 5.96473e-06
ACE [NCBI] 5.7336e-06
SRY [NCBI] 5.56022e-06
ADCYAP1 [NCBI] 5.40127e-06
MUC2 [NCBI] 5.15024e-06
NOSIP [NCBI] 4.89193e-06
PTGDR [NCBI] 4.83643e-06
PDE11A [NCBI] 4.83643e-06
PGD [NCBI] 4.78387e-06
ABCC9 [NCBI] 4.64102e-06
ARG1 [NCBI] 4.55606e-06
TACR2 [NCBI] 4.55606e-06
RXFP2 [NCBI] 4.47779e-06
PDPN [NCBI] 4.37087e-06
FGD1 [NCBI] 4.33764e-06
FGFBP1 [NCBI] 4.33764e-06
TBX3 [NCBI] 4.3055e-06
DSC3 [NCBI] 4.24417e-06
ENTPD1 [NCBI] 4.21487e-06
ROR2 [NCBI] 4.10566e-06
DSC1 [NCBI] 3.89673e-06
PTGER3 [NCBI] 3.87603e-06
NRTN [NCBI] 3.77857e-06
PRKG1 [NCBI] 3.70701e-06
RBMY1A1 [NCBI] 3.6899e-06
DRD1 [NCBI] 3.67309e-06
PTGER2 [NCBI] 3.6403e-06
TACR1 [NCBI] 3.59309e-06
POSTN [NCBI] 3.59309e-06
AHR [NCBI] 3.53106e-06
KCNJ11 [NCBI] 3.51912e-06
ALOX5 [NCBI] 3.33758e-06
MC4R [NCBI] 3.29136e-06
GH1 [NCBI] 3.25808e-06
GDF5 [NCBI] 3.22591e-06
TRPC6 [NCBI] 3.16458e-06
BDNF [NCBI] 3.11147e-06
FGF10 [NCBI] 3.1069e-06
GLI3 [NCBI] 2.87566e-06
DAZ1 [NCBI] 2.75187e-06
JUP [NCBI] 2.72641e-06
INSL3 [NCBI] 2.67745e-06
CRP [NCBI] 2.67745e-06
VASP [NCBI] 2.6715e-06
DSP [NCBI] 2.60291e-06
ACHE [NCBI] 2.58143e-06
APOD [NCBI] 2.50853e-06
PTGER1 [NCBI] 2.44582e-06
PRKCI [NCBI] 2.44116e-06
EGF [NCBI] 2.26842e-06
CAT [NCBI] 2.26437e-06
DIABLO [NCBI] 2.21186e-06
ESR2 [NCBI] 2.20463e-06
ARNT [NCBI] 2.17979e-06
KCNJ8 [NCBI] 2.13203e-06
VWF [NCBI] 2.11347e-06
CD1D [NCBI] 2.08981e-06
PTN [NCBI] 2.04343e-06
CTNNB1 [NCBI] 2.03092e-06
PGR [NCBI] 1.9993e-06
CTNNA1 [NCBI] 1.98789e-06
CBL [NCBI] 1.94907e-06
INS [NCBI] 1.94096e-06
ADM [NCBI] 1.94096e-06
TNFRSF10A [NCBI] 1.89894e-06
CD209 [NCBI] 1.86127e-06
PXN [NCBI] 1.74621e-06
GJB2 [NCBI] 1.65814e-06
SHH [NCBI] 1.637e-06
BMP7 [NCBI] 1.62007e-06
SMAD2 [NCBI] 1.59621e-06
PYY [NCBI] 1.56077e-06
AVP [NCBI] 1.54807e-06
SMAD4 [NCBI] 1.51353e-06
NOG [NCBI] 1.45803e-06
PDGFA [NCBI] 1.44434e-06
GJB1 [NCBI] 1.4046e-06
HMOX1 [NCBI] 1.37776e-06
PTPN11 [NCBI] 1.3736e-06
GAPDH [NCBI] 1.2997e-06
CNTF [NCBI] 1.24613e-06
PRKCB [NCBI] 1.19381e-06
PTEN [NCBI] 9.43416e-07
CDKN1A [NCBI] 9.41257e-07
TNFSF10 [NCBI] 6.10022e-07
CASP3 [NCBI] 5.55102e-07
BCL2L1 [NCBI] 5.42369e-07
TRH [NCBI] 4.86892e-07
CHAT [NCBI] 4.05703e-07
EPO [NCBI] 3.5328e-07
MPO [NCBI] 3.34459e-07
AKT1 [NCBI] 2.79945e-07
CCK [NCBI] 2.15383e-07
PTGS2 [NCBI] 1.40327e-07
EGFR [NCBI] 1.39949e-07



OMIM


 OMIM Link Information
gain		 01
robinow syndrome, autosomal dominant [NCBI] 0.00514373
urogenital adysplasia, hereditary [NCBI] 0.00107998
hypoadrenocorticism, familial [NCBI] 0.00101206
acromial dimples [NCBI] 0.000879846
popliteal pterygium syndrome, lethal type [NCBI] 0.000879846
baculum, congenital absence of [NCBI] 0.000610928
brachyphalangy, polydactyly, and tibial aplasia/hypoplasia [NCBI] 0.000547219
LSA [NCBI] 0.000467756
intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies [NCBI] 0.000328034
AIS [NCBI] 0.000327317
AR [NCBI] 0.000284696
FSHMD1A [NCBI] 0.000259074
PPSH [NCBI] 0.000239939
SRS [NCBI] 0.000232149
emphysema, congenital, with deafness, penoscrotal web, and mental retardation [NCBI] 0.00020291
venular insufficiency, systemic [NCBI] 0.00020291
craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis [NCBI] 0.00020291
VEGF [NCBI] 0.000194946
sotos syndrome [NCBI] 0.000188421
anal atresia, hypospadias, and penoscrotal inversion [NCBI] 0.000139246
acrorenal-mandibular syndrome [NCBI] 0.000132109
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency [NCBI] 0.000132109
disorganization, mouse, homolog of [NCBI] 0.000117663
frontonasal dysplasia [NCBI] 0.000114134
hand-foot-uterus syndrome [NCBI] 0.000108185
FFS [NCBI] 0.000105627
VIP [NCBI] 0.00010168
growth hormone insensitivity syndrome [NCBI] 9.38571e-05
UMS [NCBI] 9.08338e-05
robinow syndrome, autosomal recessive [NCBI] 8.94383e-05
NOS1 [NCBI] 8.91601e-05
MRXHF1 [NCBI] 8.68437e-05
ACLS [NCBI] 8.44741e-05
RBS [NCBI] 8.33622e-05
faciogenital dysplasia [NCBI] 8.02757e-05
AHC [NCBI] 7.83973e-05
NPY [NCBI] 7.45531e-05
SCS [NCBI] 7.42046e-05
BRRS [NCBI] 7.34392e-05
fragile x mental retardation syndrome [NCBI] 4.71968e-05
LHCGR [NCBI] 4.59151e-05
SLC18A3 [NCBI] 4.51676e-05
NOS3 [NCBI] 4.4937e-05
SRD5A2 [NCBI] 3.25098e-05
ROCK1 [NCBI] 3.13092e-05
MC5R [NCBI] 3.13092e-05
DSC3 [NCBI] 2.93848e-05
SHH [NCBI] 2.79107e-05
CYP11B1 [NCBI] 2.78722e-05
TBX3 [NCBI] 2.66263e-05
ME2 [NCBI] 2.66263e-05
RHOA [NCBI] 2.60771e-05
NRTN [NCBI] 2.24448e-05
AMH [NCBI] 2.07018e-05
MC4R [NCBI] 1.88449e-05
APOD [NCBI] 1.71953e-05
KLK3 [NCBI] 1.59615e-05
ARNT [NCBI] 1.47703e-05
GDNF [NCBI] 1.4672e-05
ESD [NCBI] 1.24194e-05
FA [NCBI] 1.21165e-05
VASP [NCBI] 1.00638e-05
TH [NCBI] 9.70739e-06
ADCYAP1 [NCBI] 9.10112e-06
PRL [NCBI] 7.67561e-06
AHR [NCBI] 7.59754e-06
ACE [NCBI] 7.48253e-06
PGR [NCBI] 7.45286e-06
NGFB [NCBI] 4.95702e-06
GJA1 [NCBI] 4.43567e-06
EGF [NCBI] 3.46579e-06
GAL [NCBI] 3.19192e-06
CCK [NCBI] 3.01333e-06
PYY [NCBI] 2.47508e-06
MPO [NCBI] 1.50585e-06
GAPDH [NCBI] 1.496e-06
CAT [NCBI] 1.49578e-06
BDNF [NCBI] 1.31497e-06
EPO [NCBI] 1.24802e-06
CNTF [NCBI] 1.0814e-06
CHAT [NCBI] 9.4222e-07
ACHE [NCBI] 2.2126e-07
AVP [NCBI] 1.63327e-07



Database Center for Life Science