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01 Werner Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
WRN [NCBI] 0.00315701
TRNL1 [NCBI] 0.000287562
RECQL [NCBI] 0.000258189
RECQL4 [NCBI] 6.43007e-05
RPA1 [NCBI] 6.32945e-05
BLM [NCBI] 5.52589e-05
WRNIP1 [NCBI] 4.53774e-05
XRCC5 [NCBI] 3.8038e-05
LMNA [NCBI] 3.35526e-05
RAD51 [NCBI] 2.4888e-05
RBPMS [NCBI] 2.4158e-05
POLD2 [NCBI] 2.4158e-05
FEN1 [NCBI] 2.23809e-05
RECQL5 [NCBI] 2.02481e-05
DHX9 [NCBI] 1.92542e-05
PARP1 [NCBI] 1.85896e-05
EFEMP1 [NCBI] 1.47192e-05
POLB [NCBI] 1.40964e-05
GSR [NCBI] 1.40028e-05
GTF2E2 [NCBI] 1.37152e-05
DCTN6 [NCBI] 1.37152e-05
TAGLN [NCBI] 1.25301e-05
H2AFX [NCBI] 1.11936e-05
SIRT6 [NCBI] 1.04374e-05
POLR1C [NCBI] 1.04374e-05
SLC20A1 [NCBI] 9.07599e-06
PRKAR1B [NCBI] 8.78904e-06
MRE11A [NCBI] 8.63374e-06
LOXL2 [NCBI] 7.96681e-06
NHEJ1 [NCBI] 7.81107e-06
PCNA [NCBI] 7.59333e-06
GIPC1 [NCBI] 7.41458e-06
MUS81 [NCBI] 7.19379e-06
NR1H2 [NCBI] 6.99844e-06
RAD18 [NCBI] 6.66457e-06
ZMPSTE24 [NCBI] 6.45136e-06
CCNT1 [NCBI] 5.889e-06
KAT2B [NCBI] 5.79605e-06
TERF2 [NCBI] 5.66563e-06
UBE2I [NCBI] 5.43189e-06
XRCC6 [NCBI] 5.39593e-06
VCP [NCBI] 5.1333e-06
LAMA1 [NCBI] 4.70763e-06
OCA2 [NCBI] 4.6388e-06
XRCC4 [NCBI] 4.50928e-06
IDS [NCBI] 4.40872e-06
TP53BP1 [NCBI] 4.05943e-06
SIRT1 [NCBI] 4.04381e-06
COL3A1 [NCBI] 4.04381e-06
G6PD [NCBI] 3.63535e-06
SOD2 [NCBI] 2.87504e-06
IGFBP3 [NCBI] 2.52727e-06
NBN [NCBI] 2.20232e-06
ATR [NCBI] 2.12333e-06
PRNP [NCBI] 2.11907e-06
PRKDC [NCBI] 2.07726e-06
SLC2A1 [NCBI] 1.78729e-06
ADIPOQ [NCBI] 1.73904e-06
PSEN2 [NCBI] 1.72337e-06
CDKN1A [NCBI] 1.69552e-06
ATM [NCBI] 1.64793e-06
MYC [NCBI] 1.6105e-06
DHFR [NCBI] 1.60202e-06
NME1 [NCBI] 1.27427e-06
TP53 [NCBI] 9.88341e-07
MSH2 [NCBI] 4.88338e-07
EGF [NCBI] 1.44671e-07



OMIM


 OMIM Link Information
gain		 01
WRN [NCBI] 0.00866756
RECQL2 [NCBI] 0.00250868
tibia, hypoplasia of, with polydactyly [NCBI] 0.00078076
porokeratosis of mibelli [NCBI] 0.000765046
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging [NCBI] 0.000725612
HGPS [NCBI] 0.000332714
growth factors, combined defect of [NCBI] 0.000223236
RTS [NCBI] 0.000214435
LMNA [NCBI] 0.000194991
BLM [NCBI] 0.000194318
RA [NCBI] 0.000193573
RECQL4 [NCBI] 0.00017618
RECQL3 [NCBI] 0.000139571
LOXL2 [NCBI] 0.000136254
SLE [NCBI] 0.000133998
POLB [NCBI] 0.000121793
arthropathy, tendinous calcinosis, and progeroid features [NCBI] 0.000111529
rapadilino syndrome [NCBI] 8.06076e-05
LDHCP [NCBI] 8.06076e-05
GSR [NCBI] 7.97459e-05
rna-binding protein gene with multiple splicing [NCBI] 7.75317e-05
PPP2CB [NCBI] 7.75317e-05
GTF2E2 [NCBI] 7.75317e-05
WRNIP1 [NCBI] 7.75317e-05
RECQL [NCBI] 7.75317e-05
acrogeria, gottron type [NCBI] 7.51158e-05
progeroid short stature with pigmented nevi [NCBI] 7.10365e-05
FEN1 [NCBI] 5.51838e-05
POLD1 [NCBI] 5.51838e-05
EFEMP1 [NCBI] 5.26761e-05
MMP1 [NCBI] 3.97898e-05
VCP [NCBI] 3.12039e-05
NRG1 [NCBI] 2.80645e-05
FGFR1 [NCBI] 2.37134e-05
G6PD [NCBI] 1.57945e-05
PCNA [NCBI] 1.15209e-05
SOD2 [NCBI] 1.01553e-05
DHFR [NCBI] 7.8597e-06
FA [NCBI] 1.85175e-06
EGF [NCBI] 1.52275e-07



Database Center for Life Science