aplnr apelin receptor
Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
|absent intersomitic vessel (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.
|Manual annotations: aplnr assayed (2 sources)|
|Computed annotations: aplnr assayed (20 sources)|
These are short form descriptions of experiments using reagents targeting the gene of interest.
|Xla Wt + aplnr MO (1 source)|
|Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (19 sources):
abnormal epididymis morphology,
abnormal heart development,
abnormal kidney morphology,
abnormal maternal behavior,
abnormal myocardial fiber physiology,
abnormal seminal vesicle morphology,
abnormal systemic arterial blood pressure,
cardiovascular system phenotype,
decreased cardiac muscle contractility,
decreased fluid intake, decreased litter size, decreased urine osmolality, embryonic growth arrest, enlarged seminal vesicle, impaired exercise endurance, prenatal lethality, incomplete penetrance, preweaning lethality, incomplete penetrance, venoocclusion[+]