abnormal nonmotile primary cilium physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of a primary cilium which contains a variable array of axonemal microtubules but does not contain molecular motors; nonmotile primary cilia are found on many different cell types and function as sensory organelles that concentrate and organize sensory signaling molecules (Mammalian Phenotype Ontology, MP_0013211)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013211
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Genes

1 gene mutations causing the abnormal nonmotile primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
PKD1 polycystic kidney disease 1 (autosomal dominant)