decreased muscle mass Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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18 genes associated with the decreased muscle mass phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AP4E1 adaptor-related protein complex 4, epsilon 1 subunit
CHRNB1 cholinergic receptor, nicotinic, beta 1 (muscle)
CHRNE cholinergic receptor, nicotinic, epsilon (muscle)
COLQ collagen-like tail subunit (single strand of homotrimer) of asymmetric acetylcholinesterase
FBN1 fibrillin 1
G6PC glucose-6-phosphatase, catalytic subunit
HDAC8 histone deacetylase 8
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
MUSK muscle, skeletal, receptor tyrosine kinase
NDN necdin, melanoma antigen (MAGE) family member
PANK2 pantothenate kinase 2
PIEZO2 piezo-type mechanosensitive ion channel component 2
RAPSN receptor-associated protein of the synapse
SMS spermine synthase
SNRPN small nuclear ribonucleoprotein polypeptide N
TBC1D20 TBC1 domain family, member 20
TGFB3 transforming growth factor, beta 3
TRIM2 tripartite motif containing 2