abnormality of the foot musculature Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the musculature of foot. (Human Phenotype Ontology, HP_0001436)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001436
Similar Terms
Downloads & Tools


29 genes associated with the abnormality of the foot musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AARS alanyl-tRNA synthetase
CRYAB crystallin, alpha B
DES desmin
DNAJB2 DnaJ (Hsp40) homolog, subfamily B, member 2
EGR2 early growth response 2
FHL1 four and a half LIM domains 1
GDAP1 ganglioside induced differentiation associated protein 1
HINT1 histidine triad nucleotide binding protein 1
HNRNPDL heterogeneous nuclear ribonucleoprotein D-like
HSPB1 heat shock 27kDa protein 1
INF2 inverted formin, FH2 and WH2 domain containing
KARS lysyl-tRNA synthetase
KIF1B kinesin family member 1B
LBR lamin B receptor
LMNA lamin A/C
LRSAM1 leucine rich repeat and sterile alpha motif containing 1
LYST lysosomal trafficking regulator
MFN2 mitofusin 2
MPZ myelin protein zero
MYH7 myosin, heavy chain 7, cardiac muscle, beta
NEFL neurofilament, light polypeptide
PMP22 peripheral myelin protein 22
PRX periaxin
RAB7A RAB7A, member RAS oncogene family
SBF2 SET binding factor 2
SMCHD1 structural maintenance of chromosomes flexible hinge domain containing 1
TCAP titin-cap
TRPV4 transient receptor potential cation channel, subfamily V, member 4
TTN titin