Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Appendix [NCBI]

Gene


 Gene Link Information
Gain		 01
SIGLEC16 [NCBI] 0.000483787
CTNNB1 [NCBI] 9.89569e-06
SIGLEC11 [NCBI] 8.83299e-06
DNTT [NCBI] 7.13806e-06
UHRF1 [NCBI] 6.46281e-06
CD68 [NCBI] 6.37508e-06
KRT19 [NCBI] 6.14241e-06
CA2 [NCBI] 5.74136e-06
TNFRSF6B [NCBI] 5.6369e-06
SELL [NCBI] 5.41544e-06
ALOX5 [NCBI] 5.31476e-06
PPIB [NCBI] 5.22332e-06
MGMT [NCBI] 4.99927e-06
PODXL [NCBI] 4.99059e-06
DCC [NCBI] 4.90766e-06
VIP [NCBI] 4.85849e-06
KRAS [NCBI] 4.48593e-06
EDN1 [NCBI] 4.46532e-06
KIT [NCBI] 4.45014e-06
CCR1 [NCBI] 4.28828e-06
PRNP [NCBI] 4.24242e-06
CD22 [NCBI] 4.17168e-06
BRAF [NCBI] 3.95764e-06
MUC2 [NCBI] 3.84517e-06
MSH2 [NCBI] 3.82627e-06
FABP7 [NCBI] 3.72957e-06
NOS1 [NCBI] 3.63932e-06
NGF [NCBI] 3.62324e-06
CCR7 [NCBI] 3.61529e-06
TOP2A [NCBI] 3.5772e-06
MLH1 [NCBI] 3.50713e-06
PYY [NCBI] 3.47669e-06
PTPN6 [NCBI] 3.38044e-06
PTPN11 [NCBI] 3.27286e-06
PTHLH [NCBI] 3.17463e-06
RAG1 [NCBI] 3.05338e-06
PTGS1 [NCBI] 3.03774e-06
CD38 [NCBI] 2.84976e-06
LPL [NCBI] 2.38548e-06
NOS2 [NCBI] 2.24054e-06
TP53 [NCBI] 2.09667e-06
PTGS2 [NCBI] 1.64556e-06
TNF [NCBI] 7.74092e-07



OMIM


 OMIM Link Information
gain		 01
immune defect due to absence of thymus [NCBI] 0.00154746
NPC1 [NCBI] 0.000228343
SCN1 [NCBI] 0.000133873
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-positive [NCBI] 0.000124096
sandhoff disease [NCBI] 0.000108628
CF [NCBI] 0.000102584
SIGLEC11 [NCBI] 5.97454e-05
UHRF1 [NCBI] 5.17116e-05
PODXL [NCBI] 4.80245e-05
PPIB [NCBI] 3.92142e-05
TNFRSF6B [NCBI] 3.92142e-05
thrombocytopenic purpura, autoimmune [NCBI] 3.52921e-05
CJD [NCBI] 3.29405e-05
CEACAM5 [NCBI] 2.7819e-05
VIP [NCBI] 2.1061e-05
PYY [NCBI] 1.77333e-05
NGFB [NCBI] 1.28969e-05
TNFSF6 [NCBI] 1.13787e-05
LPL [NCBI] 1.01713e-05
RA [NCBI] 5.07452e-06
TNF [NCBI] 1.05358e-06



Database Center for Life Science