nonprogressive disorder Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003680
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Genes

15 genes associated with the nonprogressive disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP2B3 ATPase, Ca++ transporting, plasma membrane 3
CHRNB1 cholinergic receptor, nicotinic, beta 1 (muscle)
CHRNE cholinergic receptor, nicotinic, epsilon (muscle)
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
HOXB1 homeobox B1
ILDR1 immunoglobulin-like domain containing receptor 1
KRT12 keratin 12, type I
KRT3 keratin 3, type II
MUSK muscle, skeletal, receptor tyrosine kinase
RAPSN receptor-associated protein of the synapse
RYR1 ryanodine receptor 1 (skeletal)
SEPN1 selenoprotein N, 1
TRPV4 transient receptor potential cation channel, subfamily V, member 4
VLDLR very low density lipoprotein receptor
ZNF592 zinc finger protein 592