neck flexor weakness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Weakness of the muscles involved in neck flexion (sternocleidomastoid, longus capitus, longus colli, and scalenus anterior). (Human Phenotype Ontology, HP_0003722)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003722
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Genes

7 genes associated with the neck flexor weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTA1 actin, alpha 1, skeletal muscle
CNBP CCHC-type zinc finger, nucleic acid binding protein
KBTBD13 kelch repeat and BTB (POZ) domain containing 13
MYOT myotilin
NEB nebulin
TRIM32 tripartite motif containing 32
TTN titin