rps20 Phenotypes

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Phenotypes

Gene Literature (3)

Nucleotides (1375)

Interactants (364)

XB-GENEPAGE-1001338

Gene Symbol: rps20 Gene Name: ribosomal protein S20

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (50 sources): Abdominal pain, Abnormal circulating creatine concentration, Abnormal pyramidal sign, Agnosia, Amaurosis fugax, Anxiety, Attention deficit hyperactivity disorder, Basal cell carcinoma, Behavioral abnormality, Benign neoplasm of the central nervous system, Cardiac diverticulum, Constipation, Depression, Developmental regression, Dysarthria, Dysgraphia, Dyskinesia, Fatigue, Flexion contracture, Gait disturbance, Gastrointestinal hemorrhage, Glioblastoma multiforme, Hallucinations, Hemiplegia/hemiparesis, Hepatocellular carcinoma, Hypotonia, Increased intracranial pressure, Irritability, Malabsorption, Memory impairment, Migraine, Nausea and vomiting, Neoplasm of the colon, Neoplasm of the pancreas, Neoplasm of the rectum, Neoplasm of the skeletal system, Neoplasm of the thyroid gland, Neuroblastoma, Neurological speech impairment, Pancreatic adenocarcinoma, Paresthesia, Pituitary adenoma, Seizure, Spasticity, Stomach cancer, Urinary tract neoplasm, Uterine neoplasm, Visual field defect, Visual impairment, Weight loss [+]
Mouse (11 sources): abnormal epidermal melanocyte morphology, abnormal epidermal pigmentation, abnormal melanoblast morphology, embryonic lethality prior to organogenesis, embryonic lethality, complete penetrance, increased ear pigmentation, increased foot pad pigmentation, increased melanocyte number, increased tail pigmentation, prenatal lethality, complete penetrance, preweaning lethality, complete penetrance [+]
View all ortholog results at Monarch