Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Nucleic Acid Probes [NCBI]

Gene


 Gene Link Information
Gain		 01
KRT17P1 [NCBI] 0.000299491
KRT17P2 [NCBI] 0.000299491
RWDD2B [NCBI] 2.59079e-06
EYA4 [NCBI] 2.36393e-06
HNRNPH3 [NCBI] 2.34906e-06
AGRN [NCBI] 2.30885e-06
COL9A1 [NCBI] 2.21528e-06
ENO2 [NCBI] 2.19018e-06
KRT17 [NCBI] 2.17467e-06
UROD [NCBI] 1.99494e-06
GSR [NCBI] 1.98364e-06
SS18 [NCBI] 1.97997e-06
FGF4 [NCBI] 1.72107e-06
MBL2 [NCBI] 1.55846e-06
PDGFA [NCBI] 1.38499e-06
MLL [NCBI] 1.36679e-06
TTR [NCBI] 1.3344e-06
HFE [NCBI] 1.20572e-06
PRL [NCBI] 7.8334e-07



OMIM


 OMIM Link Information
gain		 01
BWS [NCBI] 9.38273e-05
leber optic atrophy [NCBI] 9.21207e-05
PWS [NCBI] 7.42103e-05
EYA4 [NCBI] 3.95331e-05
AGRN [NCBI] 3.95331e-05
KRT17 [NCBI] 3.85095e-05
porphyria cutanea tarda [NCBI] 2.9449e-05
MBL2 [NCBI] 2.02201e-05
CF [NCBI] 1.86004e-05
TTR [NCBI] 1.57327e-05
PRL [NCBI] 5.35822e-06



Database Center for Life Science