Broad Hallux Phalanx Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An increase in width in one or more phalanges of the big toe. (Human Phenotype Ontology, HP_0010059)
External Link https://www.disgenet.org/browser/0/1/0/C4021343
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Genes

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

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
BMP2 bone morphogenetic protein 2
DACT1 dishevelled-binding antagonist of beta-catenin 1
EFNB1 ephrin-B1
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FLI1 Fli-1 proto-oncogene, ETS transcription factor
GATA4 GATA binding protein 4
GLI3 GLI family zinc finger 3
GPC4 glypican 4
KCNJ8 potassium channel, inwardly rectifying subfamily J, member 8
NXN nucleoredoxin
ROR2 receptor tyrosine kinase-like orphan receptor 2
SALL1 spalt-like transcription factor 1
SALL4 spalt-like transcription factor 4
SATB2 SATB homeobox 2
SUMF1 sulfatase modifying factor 1