Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Genetic Drift [NCBI]

Gene


 Gene Link Information
Gain		 01
TRNL1 [NCBI] 0.000135654
USP26 [NCBI] 3.87001e-06
GRASP [NCBI] 3.83748e-06
ERVWE1 [NCBI] 3.32723e-06
BSCL2 [NCBI] 3.26969e-06
RHD [NCBI] 3.06903e-06
KRIT1 [NCBI] 2.99933e-06
RHCE [NCBI] 2.95666e-06
HEXA [NCBI] 2.95666e-06
ABO [NCBI] 2.91352e-06
ERCC4 [NCBI] 2.77003e-06
ADH1B [NCBI] 2.68291e-06
APEX1 [NCBI] 2.65879e-06
MSH3 [NCBI] 2.61195e-06
CYP2E1 [NCBI] 2.44242e-06
XRCC1 [NCBI] 2.32153e-06
ALDH2 [NCBI] 2.27791e-06
ERCC2 [NCBI] 2.24279e-06
HP [NCBI] 2.21107e-06
HLA-DQB1 [NCBI] 1.96537e-06
CYP2C19 [NCBI] 1.93779e-06
G6PD [NCBI] 1.8834e-06
APC [NCBI] 1.85788e-06
ACE [NCBI] 1.81047e-06
MLH1 [NCBI] 1.6897e-06



OMIM


 OMIM Link Information
gain		 01
TSD [NCBI] 0.000262742
HSAN3 [NCBI] 0.000215513
canavan disease [NCBI] 0.000107086
mucolipidosis iv [NCBI] 0.000105132
niemann-pick disease, type a [NCBI] 0.000104223
DFNB1 [NCBI] 0.000100951
cystinuria [NCBI] 9.74962e-05
glycogen storage disease vii [NCBI] 9.68716e-05
lactase persistence [NCBI] 9.45527e-05
HHF1 [NCBI] 9.34872e-05
DYT1 [NCBI] 9.05954e-05
APC [NCBI] 9.00429e-05
gaucher disease, type i [NCBI] 8.41415e-05
BLM [NCBI] 7.92801e-05
hypercholesterolemia, autosomal dominant [NCBI] 7.37828e-05
leber optic atrophy [NCBI] 6.2989e-05
MCM6 [NCBI] 4.05605e-05
pta deficiency [NCBI] 3.55954e-05
ADH2 [NCBI] 3.53752e-05
ALDH2 [NCBI] 3.33754e-05
FANCC [NCBI] 3.3223e-05
MTTL1 [NCBI] 2.89952e-05
HEXA [NCBI] 2.81709e-05
BRCA2 [NCBI] 2.58645e-05
apc gene [NCBI] 2.44108e-05
GJB2 [NCBI] 2.3861e-05
BRCA1 [NCBI] 2.26142e-05
SOD1 [NCBI] 2.16711e-05
CRC [NCBI] 1.94393e-05
G6PD [NCBI] 1.28969e-05
CF [NCBI] 3.32939e-06



Database Center for Life Science