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01 Placenta Diseases [NCBI]


Gene


Gene Link Information
Gain
01
PIH [NCBI] 3.65676e-05
TFPI2 [NCBI] 1.59965e-05
AFP [NCBI] 1.57846e-05
VEGFA [NCBI] 1.55801e-05
SOCS3 [NCBI] 1.37577e-05
FLT1 [NCBI] 1.28865e-05
SLC38A1 [NCBI] 1.22318e-05
HSPA6 [NCBI] 1.13527e-05
SLC2A1 [NCBI] 1.11466e-05
HSD3B1 [NCBI] 1.04753e-05
IL1RAP [NCBI] 9.99877e-06
PRDX3 [NCBI] 9.39216e-06
C5AR1 [NCBI] 8.59115e-06
SOCS2 [NCBI] 8.50215e-06
LHCGR [NCBI] 8.50215e-06
SLC2A3 [NCBI] 7.74434e-06
CXCL13 [NCBI] 7.48675e-06
HSPA1A [NCBI] 7.4396e-06
CD68 [NCBI] 7.2942e-06
INHBA [NCBI] 7.26309e-06
SERPINA3 [NCBI] 7.24226e-06
PTX3 [NCBI] 7.1614e-06
ICAM3 [NCBI] 7.01041e-06
NOS2 [NCBI] 6.89422e-06
HDC [NCBI] 6.4343e-06
FCGR2A [NCBI] 6.10825e-06
SOCS1 [NCBI] 5.96621e-06
CDKN1C [NCBI] 5.89946e-06
SLC11A1 [NCBI] 4.94919e-06
ADRB2 [NCBI] 4.94392e-06
CASP3 [NCBI] 4.75039e-06
ALK [NCBI] 4.64196e-06
TF [NCBI] 4.47172e-06
IFNG [NCBI] 4.38349e-06
IL4 [NCBI] 4.35757e-06
ADAMTS13 [NCBI] 4.16068e-06
TLR2 [NCBI] 3.99409e-06
PGR [NCBI] 3.96506e-06
SHBG [NCBI] 3.81949e-06
ESR1 [NCBI] 3.61552e-06
IL10 [NCBI] 3.15641e-06
TLR4 [NCBI] 2.9095e-06
NOS3 [NCBI] 2.52788e-06
TNF [NCBI] 1.95399e-06
BAX [NCBI] 1.89458e-06
PTGS2 [NCBI] 1.02322e-06
EGF [NCBI] 9.18821e-07




OMIM


OMIM Link Information
gain
01
AOS [NCBI] 0.00063536
SRS [NCBI] 0.000460245
BWS [NCBI] 0.00034601
camptomelic syndrome, long-limb type [NCBI] 0.000107702
PROCR [NCBI] 9.81163e-05
chondrodysplasia punctata, autosomal dominant [NCBI] 8.76406e-05
RTD [NCBI] 8.31153e-05
ichthyosis, x-linked [NCBI] 8.10157e-05
epidermolysis bullosa with pyloric atresia [NCBI] 7.89629e-05
NR2F2 [NCBI] 6.48439e-05
AFP [NCBI] 6.16904e-05
PTX3 [NCBI] 4.67926e-05
PXE [NCBI] 4.43005e-05
SOCS3 [NCBI] 4.30105e-05
HDC [NCBI] 2.93332e-05
CYP1A1 [NCBI] 2.49146e-05
hla-d histocompatibility type [NCBI] 2.43067e-05
PGR [NCBI] 1.74257e-05
SHBG [NCBI] 1.42566e-05
F3 [NCBI] 9.96453e-06
VEGF [NCBI] 9.94544e-06
TNF [NCBI] 3.26796e-06
CEACAM5 [NCBI] 8.69133e-07
EGF [NCBI] 6.90229e-07




Database Center for Life Science