abnormality of the 5th toe Gene Set
Genes
40 genes associated with the abnormality of the 5th toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ALG3
|
ALG3, alpha-1,3- mannosyltransferase
|
|
B9D1
|
B9 protein domain 1
|
|
B9D2
|
B9 protein domain 2
|
|
BMP4
|
bone morphogenetic protein 4
|
|
CC2D2A
|
coiled-coil and C2 domain containing 2A
|
|
CD96
|
CD96 molecule
|
|
CEP290
|
centrosomal protein 290kDa
|
|
DDX59
|
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59
|
|
DHCR7
|
7-dehydrocholesterol reductase
|
|
DYNC2H1
|
dynein, cytoplasmic 2, heavy chain 1
|
|
EVC
|
Ellis van Creveld protein
|
|
EVC2
|
Ellis van Creveld syndrome 2
|
|
FNBP4
|
formin binding protein 4
|
|
GLI3
|
GLI family zinc finger 3
|
|
HOXD13
|
homeobox D13
|
|
IFT140
|
intraflagellar transport 140
|
|
IFT172
|
intraflagellar transport 172
|
|
IFT80
|
intraflagellar transport 80
|
|
KCNJ2
|
potassium channel, inwardly rectifying subfamily J, member 2
|
|
KIF7
|
kinesin family member 7
|
|
LBR
|
lamin B receptor
|
|
LMBR1
|
limb development membrane protein 1
|
|
MKKS
|
McKusick-Kaufman syndrome
|
|
MKS1
|
Meckel syndrome, type 1
|
|
NEK1
|
NIMA-related kinase 1
|
|
RPGRIP1
|
retinitis pigmentosa GTPase regulator interacting protein 1
|
|
RPGRIP1L
|
RPGRIP1-like
|
|
SALL1
|
spalt-like transcription factor 1
|
|
SC5D
|
sterol-C5-desaturase
|
|
SHH
|
sonic hedgehog
|
|
SMOC1
|
SPARC related modular calcium binding 1
|
|
TCTN2
|
tectonic family member 2
|
|
TMEM216
|
transmembrane protein 216
|
|
TMEM231
|
transmembrane protein 231
|
|
TMEM67
|
transmembrane protein 67
|
|
TTC21B
|
tetratricopeptide repeat domain 21B
|
|
WDPCP
|
WD repeat containing planar cell polarity effector
|
|
WDR19
|
WD repeat domain 19
|
|
WDR34
|
WD repeat domain 34
|
|
WDR60
|
WD repeat domain 60
|
