progressive muscle weakness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003323
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Genes

11 genes associated with the progressive muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C10ORF2 chromosome 10 open reading frame 2
COQ2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
LDB3 LIM domain binding 3
POLG polymerase (DNA directed), gamma
POLG2 polymerase (DNA directed), gamma 2, accessory subunit
PRPS1 phosphoribosyl pyrophosphate synthetase 1
PUS1 pseudouridylate synthase 1
SIL1 SIL1 nucleotide exchange factor
TNNT1 troponin T type 1 (skeletal, slow)
VAPB VAMP (vesicle-associated membrane protein)-associated protein B and C
YARS2 tyrosyl-tRNA synthetase 2, mitochondrial