lhx2 LIM homeobox 2
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: lhx2 assayed (3 sources)|
|Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (24 sources):
abnormal basal ganglion morphology,
abnormal cerebral cortex morphology,
abnormal cortical plate morphology,
abnormal eye development,
abnormal hair cycle,
abnormal hair cycle anagen phase,
abnormal neocortex morphology,
abnormal olfactory cortex morphology,
abnormal optic vesicle formation,
abnormal telencephalon development, abnormal telencephalon morphology, absent hippocampus, absent optic placodes, aphakia, decreased hair follicle number, decreased hematocrit, forebrain hypoplasia, lethality throughout fetal growth and development, complete penetrance, liver hypoplasia, nervous system phenotype, small liver, underdeveloped hair follicles, vision/eye phenotype[+]