Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Phosphorylase Kinase	[NCBI]

Gene	Link	Information Gain
PHKG1P3	[NCBI]	0.000264782
PHKG1P2	[NCBI]	0.000264782
PHKBP2	[NCBI]	0.000264782
PHKBP1	[NCBI]	0.000264782
PHKG1P1	[NCBI]	0.000264782
PHKA1P1	[NCBI]	0.000230073
PHKA2	[NCBI]	5.06872e-05
PHKG1	[NCBI]	2.95185e-05
PHKB	[NCBI]	2.8642e-05
PHKA1	[NCBI]	2.56429e-05
PHKG2	[NCBI]	2.5007e-05
PPP1R2	[NCBI]	7.30348e-06
CALM1	[NCBI]	3.14165e-06
PRKACA	[NCBI]	2.82082e-06
GSK3B	[NCBI]	2.80922e-06
PRKCB	[NCBI]	2.25649e-06
CTRC	[NCBI]	2.226e-06
GYS2	[NCBI]	2.16269e-06
PLN	[NCBI]	2.14186e-06
GYG2	[NCBI]	2.03165e-06
TNNI2	[NCBI]	1.8687e-06
GYS1	[NCBI]	1.84192e-06
MARK1	[NCBI]	1.80252e-06
SLC2A2	[NCBI]	1.76182e-06
PRKAG2	[NCBI]	1.73207e-06
PGM1	[NCBI]	1.68567e-06
PPP1R8	[NCBI]	1.65869e-06
SLC37A4	[NCBI]	1.58447e-06
GYG1	[NCBI]	1.52645e-06
CAMK2A	[NCBI]	1.52129e-06
ENPP1	[NCBI]	1.33299e-06
PRKCD	[NCBI]	1.04717e-06
MAPT	[NCBI]	1.00999e-06
CDK2	[NCBI]	7.93621e-07
MBP	[NCBI]	6.66932e-07

OMIM	Link	Information gain
glycogen storage disease ixa	[NCBI]	0.00151124
SRS	[NCBI]	0.00149661
muscle glycogenosis, x-linked	[NCBI]	0.000886304
phosphorylase kinase deficiency of liver and muscle, autosomal recessive	[NCBI]	0.000852479
glycogen storage disease of heart, lethal congenital	[NCBI]	0.00075527
PHKA1	[NCBI]	0.00038834
PHKB	[NCBI]	0.000360297
PHKG2	[NCBI]	0.000245593
glycogen storage disease v	[NCBI]	0.000203025
PHKG1	[NCBI]	0.000122401
mitochondrial myopathy	[NCBI]	0.000121336
cardiomyopathy, familial hypertrophic, with wolff-parkinson-white syndrome	[NCBI]	0.000121336
danon disease	[NCBI]	9.88142e-05
glycogen storage disease iii	[NCBI]	8.94118e-05
glycogen storage disease vii	[NCBI]	8.15665e-05
glycogen storage disease ii	[NCBI]	6.46999e-05
SLC2A2	[NCBI]	4.16301e-05
PRKCB1	[NCBI]	2.93641e-05
TRIP10	[NCBI]	2.85978e-05
glycogen storage disease vi	[NCBI]	2.79279e-05
PRKAG2	[NCBI]	2.5866e-05
PGM1	[NCBI]	1.79362e-05
PGK1	[NCBI]	1.74805e-05
XIST	[NCBI]	1.70616e-05
GPI	[NCBI]	8.3397e-06
MBP	[NCBI]	5.80729e-07