tp53rk Phenotypes

Phenotypes

XB-GENEPAGE-484887

Gene Symbol: tp53rk Gene Name: TP53 regulating kinase

Anatomical Phenotypes Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
abnormal eye morphology (3 sources), abnormal head morphology (2 sources), decreased size of the eye (2 sources), decreased size of the head (2 sources), abnormal cartilage tissue (1 source), abnormal retina (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.
Galloway-Mowat syndrome 1 (3AP sources), microphthalmia (3AP sources)

Experiments (Reagents) These are short form descriptions of experiments using reagents targeting the gene of interest.
Xla Wt + tp53rk MO (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (39 sources): Abnormal intervertebral disk morphology, Abnormality of immune system physiology, Abnormality of neuronal migration, Abnormality of the dentition, Adducted thumb, Aqueductal stenosis, Camptodactyly of finger, Cerebellar hypoplasia, Cerebral atrophy, Cognitive impairment, Delayed speech and language development, Diffuse mesangial sclerosis, EEG abnormality, Feeding difficulties, Generalized hypotonia, Global developmental delay, Glomerular sclerosis, Hemiplegia/hemiparesis, Hiatus hernia, Hypertelorism, Hypoplasia of the ear cartilage, Hypotelorism, Hypotonia, Intrauterine growth retardation, Macrotia, Microcephaly, Micrognathia, Nephropathy, Nephrotic syndrome, Pachygyria, Polymicrogyria, Premature birth, Proteinuria, Seizure, Short stature, Spasticity, Stage 5 chronic kidney disease, Tapered finger, Visual impairment [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Human (39 sources): Abnormal intervertebral disk morphology, Abnormality of immune system physiology, Abnormality of neuronal migration, Abnormality of the dentition, Adducted thumb, Aqueductal stenosis, Camptodactyly of finger, Cerebellar hypoplasia, Cerebral atrophy, Cognitive impairment, [+]