abnormal bone collagen fibril morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Any structural anomaly of the connective tissue bundles in the extracellular matrix of bone tissue that are composed of collagen, and play a role in tissue strength and elasticity. (Human Phenotype Ontology, HP_0011862)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011642
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Genes

3 gene mutations causing the abnormal bone collagen fibril morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BGN biglycan
PRDM5 PR domain containing 5
SUCO SUN domain containing ossification factor