mrps22 Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (134)

Interactants (47)

XB-GENEPAGE-1000282

Gene Symbol: mrps22 Gene Name: mitochondrial ribosomal protein S22

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (46 sources): Abnormal renal tubule morphology, Abnormality of metabolism/homeostasis, Abnormality of secondary sexual hair, Abnormality of the amniotic fluid, Aplasia/Hypoplasia of the breasts, Aplasia/hypoplasia of the uterus, Arachnodactyly, Ascites, Ataxia, Axial hypotonia, Decreased fertility, Decreased serum estradiol, Delayed myelination, Delayed puberty, Delayed skeletal maturation, Edema, Generalized hypotonia, Gonadal dysgenesis, Growth delay, Hearing impairment, Hypertrophic cardiomyopathy, Hypoplasia of the corpus callosum, Hypoplasia of the uterus, Hypotonia, Increased circulating gonadotropin level, Increased circulating lactate concentration, Leukoencephalopathy, Low-set ears, Metabolic acidosis, Microcephaly, Osteopenia, Osteoporosis of vertebrae, Posteriorly rotated ears, Premature ovarian insufficiency, Primary amenorrhea, Psychomotor retardation, Pulmonary fibrosis, Reduced bone mineral density, Redundant neck skin, Retrognathia, Secondary amenorrhea, Seizure, Short stature, Sparse pubic hair, Spastic tetraplegia, Streak ovary [+]
Mouse (14 sources): abnormal embryo size, decreased body length, decreased bone mineral content, decreased heart rate variability, decreased lean body mass, embryonic growth arrest, embryonic growth retardation, embryonic lethality prior to organogenesis, embryonic lethality, complete penetrance, failure of primitive streak formation, failure to gastrulate, increased total body fat amount, prenatal lethality, complete penetrance, preweaning lethality, complete penetrance [+]
View all ortholog results at Monarch