abnormal spinal cord central canal morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the ependyma-lined lumen of the spinal cord that is filled with cerebrospinal fluid; it is patent with the ventricular system of the brain and frequently becomes occluded in aging adults (Mammalian Phenotype Ontology, MP_0009688)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009688
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Genes

3 gene mutations causing the abnormal spinal cord central canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CITED2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
NAPA N-ethylmaleimide-sensitive factor attachment protein, alpha
RAB23 RAB23, member RAS oncogene family