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Summary Expression Phenotypes Gene Literature (27) GO Terms (8) Nucleotides (101) Proteins (37) Interactants (332) Wiki

emx2     empty spiracles homeobox 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: emx2 assayed (20 sources)
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (13 sources): Agenesis of corpus callosum, Aplasia/Hypoplasia of the corpus callosum, Cerebral cortical atrophy, EEG abnormality, Global developmental delay, Hemiparesis, Intellectual disability, Porencephalic cyst, Schizencephaly, Seizure, [+]
Mouse (53 sources): Wolffian duct degeneration, abnormal Ammon gyrus morphology, abnormal axon extension, abnormal cerebral cortex morphology, abnormal cerebral hemisphere morphology, abnormal cochlea morphology, abnormal cochlear inner hair cell morphology, abnormal hippocampal fimbria morphology, abnormal incudomalleolar joint morphology, abnormal incudostapedial joint morphology, [+]

View all ortholog results at Monarch