copb2 Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (323)

Interactants (63)

XB-GENEPAGE-964667

Gene Symbol: copb2 Gene Name: COPI coat complex subunit beta 2

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: copb2 assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (17 sources): Abnormal cortical bone morphology, Agenesis of corpus callosum, Global developmental delay, Gray matter heterotopia, Growth delay, Hyperreflexia, Hypoplasia of the frontal lobes, Intellectual disability, severe, Microcephaly, Pachygyria, Short stature, Sloping forehead, Thin upper lip vermilion, Unilateral renal agenesis, Upslanted palpebral fissure, Ventriculomegaly, Vesicoureteral reflux [+]
Mouse (17 sources): abnormal cerebral cortex morphology, abnormal embryo size, abnormal head size, abnormal neuron proliferation, abnormal retina vasculature morphology, abnormal suckling behavior, decreased birth body size, decreased brain weight, embryonic lethality between implantation and placentation, embryonic lethality prior to tooth bud stage, increased lean body mass, increased neuron apoptosis, increased neuronal precursor proliferation, no abnormal phenotype detected, prenatal lethality, preweaning lethality, complete penetrance, preweaning lethality, incomplete penetrance [+]
View all ortholog results at Monarch