absent ulna Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Missing ulna bone associated with congenital failure of development. (Human Phenotype Ontology, HP_0003982)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004360
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7 gene mutations causing the absent ulna phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP5 bone morphogenetic protein 5
FGF10 fibroblast growth factor 10
LMX1B LIM homeobox transcription factor 1, beta
RECK reversion-inducing-cysteine-rich protein with kazal motifs
TBX3 T-box 3
TP63 tumor protein p63
WNT7A wingless-type MMTV integration site family, member 7A