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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hexosamines [NCBI]

Gene


 Gene Link Information
Gain		 01
NAGK [NCBI] 8.76992e-06
GFPT1 [NCBI] 6.82382e-06
SLC2A4 [NCBI] 5.82418e-06
RENBP [NCBI] 3.97914e-06
CETP [NCBI] 3.58308e-06
VCAN [NCBI] 3.00912e-06
EIF4EBP1 [NCBI] 2.95224e-06
SLC2A1 [NCBI] 2.42911e-06
IRS1 [NCBI] 2.26411e-06
FBLN2 [NCBI] 1.987e-06
MGEA5 [NCBI] 1.96421e-06
CBLC [NCBI] 1.96421e-06
TSHB [NCBI] 1.95351e-06
TCN1 [NCBI] 1.95351e-06
MAFA [NCBI] 1.88862e-06
OGT [NCBI] 1.80457e-06
GNE [NCBI] 1.77609e-06
HSPG2 [NCBI] 1.74072e-06
GALNS [NCBI] 1.71804e-06
GLB1 [NCBI] 1.67776e-06
CGA [NCBI] 1.6632e-06
TXNIP [NCBI] 1.60891e-06
ABO [NCBI] 1.56139e-06
PODXL [NCBI] 1.52737e-06
SIGLEC1 [NCBI] 1.50886e-06
PIK3CG [NCBI] 1.44238e-06
USF1 [NCBI] 1.32825e-06
FRAP1 [NCBI] 1.30231e-06
IRS2 [NCBI] 1.26481e-06
NID1 [NCBI] 1.22847e-06
IAPP [NCBI] 1.22366e-06
CRH [NCBI] 1.21827e-06
FOXO1 [NCBI] 1.20973e-06
SP1 [NCBI] 1.19466e-06
ITGB1 [NCBI] 1.17925e-06
AGT [NCBI] 1.07299e-06
TFPI [NCBI] 1.07222e-06
UMOD [NCBI] 1.06577e-06
CAV1 [NCBI] 1.05547e-06
ALB [NCBI] 1.05332e-06
EGF [NCBI] 1.0478e-06
PRKCB [NCBI] 9.96567e-07
CTGF [NCBI] 9.85553e-07
TF [NCBI] 9.66103e-07
APOB [NCBI] 9.34225e-07
G6PD [NCBI] 9.25504e-07
PLAUR [NCBI] 8.53346e-07
HGF [NCBI] 7.05584e-07
AKT1 [NCBI] 6.84891e-07
MPO [NCBI] 6.75481e-07
TGFB1 [NCBI] 6.70618e-07
CCK [NCBI] 6.24935e-07



OMIM


 OMIM Link Information
gain		 01
gangliosidosis, gm2, type iii, or juvenile type [NCBI] 0.00264194
TSD [NCBI] 0.000406687
sialuria [NCBI] 0.00023323
mucopolysaccharidoses, unclassified types [NCBI] 0.000139612
myopathy with storage of glycoproteins and glycosaminoglycans [NCBI] 0.000139612
winchester syndrome [NCBI] 0.000121544
follicle-stimulating hormone deficiency, isolated [NCBI] 0.000114476
ACG2 [NCBI] 0.000114476
DMC [NCBI] 0.000111627
MCDS [NCBI] 0.000109097
CDG2A [NCBI] 0.000109097
gm1-gangliosidosis, type ii [NCBI] 0.000101113
galactokinase deficiency [NCBI] 9.65602e-05
ehlers-danlos syndrome, type iv, autosomal dominant [NCBI] 8.855e-05
sialuria, finnish type [NCBI] 8.67029e-05
infantile sialic acid storage disorder [NCBI] 8.67029e-05
gm1-gangliosidosis, type i [NCBI] 8.49964e-05
mannosidosis, alpha b, lysosomal [NCBI] 7.68303e-05
sandhoff disease [NCBI] 7.46609e-05
udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase [NCBI] 6.11166e-05
MGEA5 [NCBI] 3.32872e-05
ST8SIA2 [NCBI] 3.18497e-05
ST8SIA4 [NCBI] 3.02314e-05
GLB1 [NCBI] 2.35055e-05
mucopolysaccharidosis type iva [NCBI] 2.35055e-05
aspartylglucosaminuria [NCBI] 2.33755e-05
F2 [NCBI] 2.11952e-05
SLE [NCBI] 1.93897e-05
COL2A1 [NCBI] 1.93481e-05
HEXA [NCBI] 1.92885e-05
GCK [NCBI] 1.90004e-05
PAEP [NCBI] 1.84677e-05
ABCC8 [NCBI] 1.72531e-05
SLC2A4 [NCBI] 1.60738e-05
HEMB [NCBI] 1.53589e-05
MAG [NCBI] 1.04804e-05
IL2 [NCBI] 9.21279e-06
SOD2 [NCBI] 9.18094e-06
ALB [NCBI] 9.04025e-06
TFPI [NCBI] 8.74221e-06
TF [NCBI] 7.23184e-06
APOB [NCBI] 6.80259e-06
G6PD [NCBI] 5.58738e-06
NPPA [NCBI] 3.68696e-06
HGF [NCBI] 2.7325e-06
MPO [NCBI] 2.21682e-06
CCK [NCBI] 1.47704e-06
CEACAM5 [NCBI] 1.04491e-06
EGF [NCBI] 9.33928e-07
VEGF [NCBI] 9.98796e-08



Database Center for Life Science