MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
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