abnormality of the middle phalanx of the 5th finger Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004219
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Genes

14 genes associated with the abnormality of the middle phalanx of the 5th 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
GATA1 GATA binding protein 1 (globin transcription factor 1)
GDF5 growth differentiation factor 5
GJA1 gap junction protein, alpha 1, 43kDa
H19 H19, imprinted maternally expressed transcript (non-protein coding)
HOXD13 homeobox D13
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NOG noggin
RBBP8 retinoblastoma binding protein 8
ROR2 receptor tyrosine kinase-like orphan receptor 2
RUNX2 runt-related transcription factor 2
TFAP2B transcription factor AP-2 beta (activating enhancer binding protein 2 beta)
WNT5A wingless-type MMTV integration site family, member 5A