abnormal pollex morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the first or primary digit on the radial side of the hand (Mammalian Phenotype Ontology, MP_0010772)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010772
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Genes

2 gene mutations causing the abnormal pollex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MKS1 Meckel syndrome, type 1
SMOC1 SPARC related modular calcium binding 1