jun Phenotypes

Summary

Expression

Phenotypes

Gene Literature (147)

XB-GENEPAGE-482227

Gene Symbol: jun Gene Name: jun proto-oncogene

Expression Phenotypes 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: jun assayed (9 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (66 sources): abnormal allantois morphology, abnormal bile duct development, abnormal cardiac neural crest cell migration, abnormal cell proliferation, abnormal craniofacial morphology, abnormal cytokine level, abnormal eyelid development, abnormal hindbrain development, abnormal keratinocyte morphology, abnormal keratinocyte physiology, abnormal limb bud morphology, abnormal limb morphology, abnormal liver development, abnormal liver regeneration, abnormal placenta morphology, abnormal placenta vasculature, abnormal prepulse inhibition, abnormal pulmonary alveolar parenchyma morphology, abnormal pulmonary alveolar system morphology, abnormal tail morphology, abnormal truncus arteriosus septation, abnormal tumor necrosis factor level, abnormal visceral yolk sac morphology, abnormal vitelline vasculature morphology, blood vessel congestion, decreased body length, decreased body size, decreased cell proliferation, decreased cellular sensitivity to ultraviolet irradiation, decreased fibroblast proliferation, decreased hepatocyte proliferation, decreased keratinocyte proliferation, decreased liver weight, decreased neuron apoptosis, decreased susceptibility to neuronal excitotoxicity, decreased susceptibility to pharmacologically induced seizures, delayed wound healing, dissociated hepatocytes, embryonic growth retardation, embryonic lethality during organogenesis, complete penetrance, embryonic lethality during organogenesis, incomplete penetrance, enlarged lymph nodes, eye opacity, eyelids open at birth, failure of eyelid fusion, fusion of vertebral arches, impaired wound healing, improved glucose tolerance, increased hepatocyte apoptosis, increased incidence of corneal inflammation, increased lung apoptosis, increased nucleated erythrocyte cell number, increased prepulse inhibition, lethality throughout fetal growth and development, complete penetrance, liver/biliary system phenotype, neonatal lethality, complete penetrance, neonatal lethality, incomplete penetrance, nervous system phenotype, no abnormal phenotype detected, oxidative stress, perinatal lethality, incomplete penetrance, postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, prenatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, thin ventricular wall [+]

Monarch Ortholog Phenotypes

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

Mouse (66 sources): abnormal allantois morphology, abnormal bile duct development, abnormal cardiac neural crest cell migration, abnormal cell proliferation, abnormal craniofacial morphology, abnormal cytokine level, abnormal eyelid development, abnormal hindbrain development, abnormal keratinocyte morphology, abnormal keratinocyte physiology, [+]