nr1h2 Phenotypes

Phenotypes

XB-GENEPAGE-482949

Gene Symbol: nr1h2 Gene Name: nuclear receptor subfamily 1 group H member 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: nr1h2 assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (23 sources): abnormal Sertoli cell morphology, abnormal glycogen homeostasis, abnormal lipid homeostasis, abnormal lipid level, abnormal myometrium morphology, abnormal retina ganglion cell morphology, abnormal retina nerve fiber layer morphology, abnormal skeleton physiology, abnormal spermatogonia proliferation, abnormal uterus physiology, amyloid beta deposits, decreased oligodendrocyte number, decreased retina ganglion cell number, hindlimb paralysis, impaired smooth muscle contractility, increased microglial cell activation, increased muscle cell glucose uptake, increased sensitivity to induced morbidity/mortality, no abnormal phenotype detected, optic nerve degeneration, pregnancy-related premature death, reproductive system phenotype, thin epidermis [+]

Monarch Ortholog Phenotypes

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

Mouse (23 sources): abnormal Sertoli cell morphology, abnormal glycogen homeostasis, abnormal lipid homeostasis, abnormal lipid level, abnormal myometrium morphology, abnormal retina ganglion cell morphology, abnormal retina nerve fiber layer morphology, abnormal skeleton physiology, abnormal spermatogonia proliferation, abnormal uterus physiology, [+]