weak cry Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001612
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Genes

16 genes associated with the weak cry phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTA1 actin, alpha 1, skeletal muscle
CHAT choline O-acetyltransferase
CHRNA1 cholinergic receptor, nicotinic, alpha 1 (muscle)
CHRNB1 cholinergic receptor, nicotinic, beta 1 (muscle)
CHRND cholinergic receptor, nicotinic, delta (muscle)
CHRNE cholinergic receptor, nicotinic, epsilon (muscle)
COLQ collagen-like tail subunit (single strand of homotrimer) of asymmetric acetylcholinesterase
COQ9 coenzyme Q9
CRYAB crystallin, alpha B
IGHMBP2 immunoglobulin mu binding protein 2
LAMA3 laminin, alpha 3
MUSK muscle, skeletal, receptor tyrosine kinase
NIPBL Nipped-B homolog (Drosophila)
RAPSN receptor-associated protein of the synapse
SEPN1 selenoprotein N, 1
TPM3 tropomyosin 3