abnormality of the talus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the talus. (Human Phenotype Ontology, HP_0008365)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008365
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Genes

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

Symbol Name
ANOS1 anosmin 1
ARID1B AT rich interactive domain 1B (SWI1-like)
CCDC8 coiled-coil domain containing 8
CHD7 chromodomain helicase DNA binding protein 7
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
CUL7 cullin 7
DOK7 docking protein 7
DUSP6 dual specificity phosphatase 6
EMG1 EMG1 N1-specific pseudouridine methyltransferase
ERCC1 excision repair cross-complementation group 1
ERCC2 excision repair cross-complementation group 2
ERCC6 excision repair cross-complementation group 6
FAM111A family with sequence similarity 111, member A
FEZF1 FEZ family zinc finger 1
FGF17 fibroblast growth factor 17
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FLNA filamin A, alpha
FLRT3 fibronectin leucine rich transmembrane protein 3
HESX1 HESX homeobox 1
HOXD10 homeobox D10
HS6ST1 heparan sulfate 6-O-sulfotransferase 1
IL17RD interleukin 17 receptor D
KISS1R KISS1 receptor
LMNA lamin A/C
MYBPC1 myosin binding protein C, slow type
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
NSMF NMDA receptor synaptonuclear signaling and neuronal migration factor
OBSL1 obscurin-like 1
PEX1 peroxisomal biogenesis factor 1
PHEX phosphate regulating endopeptidase homolog, X-linked
PHGDH phosphoglycerate dehydrogenase
POR P450 (cytochrome) oxidoreductase
PROK2 prokineticin 2
PROKR2 prokineticin receptor 2
RAPSN receptor-associated protein of the synapse
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SETBP1 SET binding protein 1
SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10
SOX10 SRY (sex determining region Y)-box 10
SPRY4 sprouty homolog 4 (Drosophila)
TACR3 tachykinin receptor 3
TNNI2 troponin I type 2 (skeletal, fast)
TNNT3 troponin T type 3 (skeletal, fast)
TPM2 tropomyosin 2 (beta)
VIPAS39 VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog
VPS33B vacuolar protein sorting 33 homolog B (yeast)
WDR11 WD repeat domain 11
WRN Werner syndrome, RecQ helicase-like
ZMPSTE24 zinc metallopeptidase STE24