Oligodactyly Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A developmental defect resulting in the presence of fewer than the normal number of digits. (Human Phenotype Ontology, HP_0012165)
External Link https://www.disgenet.org/browser/0/1/0/C3887496
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Genes

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

Symbol Name
BTRC beta-transducin repeat containing E3 ubiquitin protein ligase
CYP26B1 cytochrome P450, family 26, subfamily B, polypeptide 1
DLX5 distal-less homeobox 5
DLX6 distal-less homeobox 6
DONSON downstream neighbor of SON
EPS15L1 epidermal growth factor receptor pathway substrate 15-like 1
GLI3 GLI family zinc finger 3
HDAC8 histone deacetylase 8
HOXD13 homeobox D13
KMT2A lysine (K)-specific methyltransferase 2A
LMBR1 limb development membrane protein 1
MBTPS2 membrane-bound transcription factor peptidase, site 2
NIPBL Nipped-B homolog (Drosophila)
RAD21 RAD21 homolog (S. pombe)
SETD5 SET domain containing 5
SHFM1 split hand/foot malformation (ectrodactyly) type 1
SMC1A structural maintenance of chromosomes 1A
SMC3 structural maintenance of chromosomes 3
TP63 tumor protein p63
WNT10B wingless-type MMTV integration site family, member 10B