Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
|abnormal development of pronephric kidney (2 sources), abnormal pronephric tubule morphology (2 sources), abnormal development of distal tubule (1 source), abnormal development of proximal tubule (1 source), abnormal pronephric kidney morphology (1 source), decreased size of the distal tubule (1 source), decreased size of the pronephric kidney (1 source), edematous embryo (1 source)|
Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
|Computed annotations: invs assayed (6 sources)|
Diseases from the human disease ontology (DO) manually associated with phenotypes from disease models. Sources are grouped by anatomical (AP) and expression (EP) phenotypes.
|nephronophthisis 2 (9AP sources)|
These are short form descriptions of experiments using reagents targeting the gene of interest.
|Xla Wt + invs MO (9 sources)|