deviation of the hallux Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Displacement of the big toe from its normal position. (Human Phenotype Ontology, HP_0010051)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010051
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Genes

34 genes associated with the deviation of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACVR1 activin A receptor, type I
AKT1 v-akt murine thymoma viral oncogene homolog 1
ATL3 atlastin GTPase 3
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
CLIP2 CAP-GLY domain containing linker protein 2
COL1A1 collagen, type I, alpha 1
COL5A1 collagen, type V, alpha 1
COL5A2 collagen, type V, alpha 2
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
ELN elastin
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GDF5 growth differentiation factor 5
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
HOXA13 homeobox A13
HOXD13 homeobox D13
IL11RA interleukin 11 receptor, alpha
LIMK1 LIM domain kinase 1
PTEN phosphatase and tensin homolog
RBBP8 retinoblastoma binding protein 8
RFC2 replication factor C (activator 1) 2, 40kDa
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
TBL2 transducin (beta)-like 2
TCF12 transcription factor 12
TP63 tumor protein p63
TWIST1 twist family bHLH transcription factor 1