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XB-GENEPAGE-5845671
camsap3 calmodulin regulated spectrin associated protein family member 3
Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology
covering anatomical, gene ontology, and neurobehavioral phenotypes.
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abnormal multiciliated cell (2 sources), obsolete decreased cilium motility in multiciliated cell (2 sources), abnormal ciliary basal body organization (1 source), abnormal establishment of epithelial cell polarity (1 source) |
Diseases
Diseases from the human disease ontology (DO) manually associated with phenotypes
from disease models. Sources are grouped by anatomical (AP) and expression (EP) phenotypes.
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primary ciliary dyskinesia (2AP sources) |
Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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Xla + camsap3 MO (3 sources) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Mouse (27 sources): abnormal adipose tissue amount, abnormal blood urea nitrogen level, abnormal body length, abnormal bone mineralization, abnormal cervical rib, abnormal circulating alkaline phosphatase level, abnormal dorsal root ganglion morphology, abnormal ductus venosus valve morphology, abnormal lean body mass, abnormal placenta morphology, [+] |