abnormal coccyx morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the rostral-most segment of the vertebral column that is formed by the fusion of three to five coccygeal vertebrae in adult humans and tailless primates (Mammalian Phenotype Ontology, MP_0010114)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010114
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Genes

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

Symbol Name
DACT1 dishevelled-binding antagonist of beta-catenin 1
PAPPA2 pappalysin 2