glycogen storage disease iv Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2750)
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Genes

22 genes co-occuring with the disease glycogen storage disease iv in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
GBE1 glucan (1,4-alpha-), branching enzyme 1 2.94002
RBCK1 RanBP-type and C3HC4-type zinc finger containing 1 1.25602
PFKM phosphofructokinase, muscle 1.09209
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit 0.960797
MYOT myotilin 0.885979
AMPD1 adenosine monophosphate deaminase 1 0.862637
NHLRC1 NHL repeat containing E3 ubiquitin protein ligase 1 0.774932
G6PC glucose-6-phosphatase, catalytic subunit 0.75412
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 0.748424
PYGB phosphorylase, glycogen; brain 0.745985
PYGL phosphorylase, glycogen, liver 0.742735
PYGM phosphorylase, glycogen, muscle 0.714811
RYBP RING1 and YY1 binding protein 0.632777
LAMP2 lysosomal-associated membrane protein 2 0.606152
LDB3 LIM domain binding 3 0.543155
ROBO2 roundabout, axon guidance receptor, homolog 2 (Drosophila) 0.511496
GAA glucosidase, alpha; acid 0.453339
HTR1F 5-hydroxytryptamine (serotonin) receptor 1F, G protein-coupled 0.436778
TPM1 tropomyosin 1 (alpha) 0.42214
POU1F1 POU class 1 homeobox 1 0.383708
GBA glucosidase, beta, acid 0.302698
ROBO1 roundabout, axon guidance receptor, homolog 1 (Drosophila) 0.254183