abnormality of the 2nd finger Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the second finger, also known as the index finger. (Human Phenotype Ontology, HP_0004100)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004100
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12 genes associated with the abnormality of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BMP2 bone morphogenetic protein 2
BMPR1B bone morphogenetic protein receptor, type IB
COL2A1 collagen, type II, alpha 1
FGFR2 fibroblast growth factor receptor 2
FLNA filamin A, alpha
GDF5 growth differentiation factor 5
HOXA13 homeobox A13
IHH indian hedgehog
IRX5 iroquois homeobox 5
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
RUNX2 runt-related transcription factor 2
TWIST1 twist family bHLH transcription factor 1