MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Glycolates
[NCBI]
Gene
Gene
Link
Information
Gain
01
AGXT2L1
[NCBI]
1.84494e-05
TDP1
[NCBI]
6.41122e-06
GRHPR
[NCBI]
6.37513e-06
BMP2
[NCBI]
5.06199e-06
PGP
[NCBI]
4.21568e-06
CLIC1
[NCBI]
4.10981e-06
PRKDC
[NCBI]
2.59831e-06
XRCC5
[NCBI]
2.53718e-06
AGXT2
[NCBI]
2.39101e-06
BPGM
[NCBI]
2.08101e-06
TREX1
[NCBI]
1.96008e-06
GSTZ1
[NCBI]
1.9154e-06
AGXT
[NCBI]
1.85001e-06
TPI1
[NCBI]
1.83134e-06
APTX
[NCBI]
1.74049e-06
DCLRE1C
[NCBI]
1.67616e-06
LIG3
[NCBI]
1.62714e-06
CFTR
[NCBI]
1.58293e-06
XRCC6
[NCBI]
1.5356e-06
KRT5
[NCBI]
1.48672e-06
ETS2
[NCBI]
1.47697e-06
APEX1
[NCBI]
1.44971e-06
CYP1B1
[NCBI]
1.35801e-06
WRN
[NCBI]
1.27013e-06
DCT
[NCBI]
1.24696e-06
IBSP
[NCBI]
1.13949e-06
BMP4
[NCBI]
1.1268e-06
FOLR1
[NCBI]
1.03492e-06
NFKB1
[NCBI]
1.00907e-06
G6PD
[NCBI]
9.51985e-07
CDK2
[NCBI]
8.74117e-07
CASP9
[NCBI]
8.29767e-07
AFP
[NCBI]
7.25361e-07
AR
[NCBI]
6.89107e-07
AVP
[NCBI]
6.72723e-07
PCNA
[NCBI]
6.44307e-07
CDKN1A
[NCBI]
5.82424e-07
CASP3
[NCBI]
5.46523e-07
PTH
[NCBI]
5.29909e-07
TNF
[NCBI]
3.40992e-07
OMIM
OMIM
Link
Information
gain
01
hyperoxaluria, primary, type i
[NCBI]
0.000857337
hyperoxaluria, primary, type ii
[NCBI]
0.000299241
hydroxyprolinemia
[NCBI]
0.000139291
PHA2
[NCBI]
0.000107087
adrenoleukodystrophy, autosomal neonatal form
[NCBI]
8.82258e-05
WRN
[NCBI]
7.81184e-05
AGXT
[NCBI]
7.12602e-05
PGP
[NCBI]
6.52657e-05
diphosphoglycerate mutase deficiency of erythrocyte
[NCBI]
3.26603e-05
CFTR
[NCBI]
2.01972e-05
CDK2
[NCBI]
1.65925e-05
SERPINA6
[NCBI]
1.61529e-05
SPP1
[NCBI]
9.87248e-06
G6PD
[NCBI]
8.50765e-06
AR
[NCBI]
5.0708e-06
VEGF
[NCBI]
5.01227e-06
AFP
[NCBI]
5.0046e-06
PCNA
[NCBI]
3.71845e-06
AVP
[NCBI]
3.27007e-06
PTH
[NCBI]
1.99772e-06
TNF
[NCBI]
3.15154e-07
CF
[NCBI]
7.87444e-08
Database Center for Life Science