fused phalanges Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly of the long bones of the digits resulting in some or all the bones being joined together (Mammalian Phenotype Ontology, MP_0008730)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008730
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12 gene mutations causing the fused phalanges phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMPR1B bone morphogenetic protein receptor, type IB
EN1 engrailed homeobox 1
FBN2 fibrillin 2
FMN1 formin 1
FREM2 FRAS1 related extracellular matrix protein 2
FSTL1 follistatin-like 1
GDF5 growth differentiation factor 5
IRF6 interferon regulatory factor 6
JAG2 jagged 2
MYO10 myosin X
PORCN porcupine homolog (Drosophila)
WNT7A wingless-type MMTV integration site family, member 7A