neck muscle weakness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Decreased strength of the neck musculature. (Human Phenotype Ontology, HP_0000467)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000467
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Genes

24 genes associated with the neck muscle 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
CAV3 caveolin 3
CFL2 cofilin 2 (muscle)
CNBP CCHC-type zinc finger, nucleic acid binding protein
CRYAB crystallin, alpha B
DES desmin
GFPT1 glutamine--fructose-6-phosphate transaminase 1
KBTBD13 kelch repeat and BTB (POZ) domain containing 13
LMNA lamin A/C
MTM1 myotubularin 1
MYH7 myosin, heavy chain 7, cardiac muscle, beta
MYOT myotilin
NEB nebulin
PABPN1 poly(A) binding protein, nuclear 1
PNPLA2 patatin-like phospholipase domain containing 2
SLC52A2 solute carrier family 52 (riboflavin transporter), member 2
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3
SYNE1 spectrin repeat containing, nuclear envelope 1
TGM6 transglutaminase 6
TMEM43 transmembrane protein 43
TPM2 tropomyosin 2 (beta)
TPM3 tropomyosin 3
TRIM32 tripartite motif containing 32
TTN titin