absent radius Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Missing radius bone associated with congenital failure of development. (Human Phenotype Ontology, HP_0003974)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000553
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Genes

7 gene mutations causing the absent radius phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGF10 fibroblast growth factor 10
GLI3 GLI family zinc finger 3
RDH10 retinol dehydrogenase 10 (all-trans)
RSPO2 R-spondin 2
SP8 Sp8 transcription factor
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TP63 tumor protein p63