Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Alkalies [NCBI]

Gene


 Gene Link Information
Gain		 01
SLC9A3 [NCBI] 4.55688e-06
EGF [NCBI] 4.19681e-06
PCNA [NCBI] 2.94329e-06
ACER1 [NCBI] 2.15614e-06
CHAT [NCBI] 2.03463e-06
SLC16A7 [NCBI] 2.03364e-06
HMMR [NCBI] 1.95804e-06
MPG [NCBI] 1.82472e-06
SLC13A2 [NCBI] 1.8149e-06
PDCD6IP [NCBI] 1.70248e-06
CFTR [NCBI] 1.66769e-06
MTF1 [NCBI] 1.56655e-06
SLC9A1 [NCBI] 1.55905e-06
VCAN [NCBI] 1.38568e-06
KCNJ8 [NCBI] 1.34049e-06
TGFBI [NCBI] 1.33968e-06
FGF2 [NCBI] 1.2738e-06
BID [NCBI] 1.23657e-06
SNAI2 [NCBI] 1.23057e-06
CHGA [NCBI] 1.2295e-06
MAPK14 [NCBI] 1.22418e-06
IBSP [NCBI] 1.18194e-06
NOG [NCBI] 1.16626e-06
APP [NCBI] 1.11594e-06
SLC2A1 [NCBI] 1.09639e-06
TTR [NCBI] 1.09509e-06
CYP2C9 [NCBI] 1.0204e-06
G6PD [NCBI] 9.94225e-07
DHFR [NCBI] 9.39668e-07
CAT [NCBI] 8.18526e-07
VEGFA [NCBI] 7.3023e-07
PTH [NCBI] 5.70455e-07
NGF [NCBI] 5.57958e-07
TNF [NCBI] 3.79099e-07



OMIM


 OMIM Link Information
gain		 01
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation [NCBI] 0.000328328
renal tubular acidosis, proximal [NCBI] 0.000174453
renal tubular acidosis, distal, autosomal dominant [NCBI] 0.000134519
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency [NCBI] 0.000105446
CF [NCBI] 6.39269e-05
CATSPER1 [NCBI] 3.91851e-05
CJD [NCBI] 3.53674e-05
MMP1 [NCBI] 2.59467e-05
MAPK3 [NCBI] 2.11535e-05
EGF [NCBI] 2.08231e-05
PCNA [NCBI] 2.00173e-05
FGF2 [NCBI] 1.69434e-05
CFTR [NCBI] 1.53896e-05
CHAT [NCBI] 1.43713e-05
TTR [NCBI] 8.5299e-06
HBB [NCBI] 7.45523e-06
VEGF [NCBI] 6.86115e-06
G6PD [NCBI] 6.23449e-06
DHFR [NCBI] 5.84615e-06
CAT [NCBI] 3.90483e-06
PTH [NCBI] 6.44534e-07
NGFB [NCBI] 4.92904e-07
TNF [NCBI] 3.36576e-08



Database Center for Life Science