Hallux Valgus Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Lateral deviation of the great toe (i.e., in the direction of the little toe). (Human Phenotype Ontology, HP_0001822)
External Link https://www.disgenet.org/browser/0/1/0/C0018536
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Genes

60 genes associated with the disease Hallux Valgus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACVR1 activin A receptor, type I
AEBP1 AE binding protein 1
AKT1 v-akt murine thymoma viral oncogene homolog 1
AMH anti-Mullerian hormone
ATL3 atlastin GTPase 3
ATP6V1B2 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B2
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
BAZ1B bromodomain adjacent to zinc finger domain, 1B
BMP2 bone morphogenetic protein 2
BMPR1B bone morphogenetic protein receptor, type IB
CHRM3 cholinergic receptor, muscarinic 3
CHST11 carbohydrate (chondroitin 4) sulfotransferase 11
CLIP2 CAP-GLY domain containing linker protein 2
COL1A2 collagen, type I, alpha 2
DMRTA1 DMRT-like family A1
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
ELN elastin
ERF Ets2 repressor factor
ERMARD ER membrane-associated RNA degradation
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FHL1 four and a half LIM domains 1
GDF5 growth differentiation factor 5
GIF gastric intrinsic factor (vitamin B synthesis)
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
GZMM granzyme M (lymphocyte met-ase 1)
HOXD13 homeobox D13
KCNH1 potassium channel, voltage gated eag related subfamily H, member 1
KCTD7 potassium channel tetramerization domain containing 7
LIMK1 LIM domain kinase 1
MLXIPL MLX interacting protein-like
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
NONO non-POU domain containing, octamer-binding
NUP107 nucleoporin 107kDa
OFD1 oral-facial-digital syndrome 1
PRDM5 PR domain containing 5
PTEN phosphatase and tensin homolog
RBBP8 retinoblastoma binding protein 8
RFC2 replication factor C (activator 1) 2, 40kDa
ROM1 retinal outer segment membrane protein 1
SCARF2 scavenger receptor class F, member 2
SF3B4 splicing factor 3b, subunit 4, 49kDa
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
SLC29A3 solute carrier family 29 (equilibrative nucleoside transporter), member 3
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
SMC1A structural maintenance of chromosomes 1A
SRY sex determining region Y
TBL2 transducin (beta)-like 2
TMEM201 transmembrane protein 201
TNF tumor necrosis factor
TP63 tumor protein p63
TPSG1 tryptase gamma 1
TRIM8 tripartite motif containing 8
TSPO translocator protein (18kDa)
TTPA tocopherol (alpha) transfer protein
TWIST1 twist family bHLH transcription factor 1
USP9X ubiquitin specific peptidase 9, X-linked
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
ZNF469 zinc finger protein 469