abnormality of the foot musculature Gene Set
Genes
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
|
