abnormal limb mesenchyme morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the primordial embryonic connective tissue of the developing limbs, autopods and digits, consisting of mesenchymal cells supported in interlaminar jelly, that derive mostly from the mesoderm and contribute to limb connective tissue, bone and musculature in conjunction with myotome cells (Mammalian Phenotype Ontology, MP_0011261)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011261
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5 gene mutations causing the abnormal limb mesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GREM1 gremlin 1, DAN family BMP antagonist
OFD1 oral-facial-digital syndrome 1
P4HA1 prolyl 4-hydroxylase, alpha polypeptide I
TCTN2 tectonic family member 2
WDR19 WD repeat domain 19