hmx2 Phenotypes

XB-GENEPAGE-480084

Gene Symbol: hmx2 Gene Name: H6 family 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: hmx2 assayed (5 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (19 sources): abnormal bone mineralization, abnormal crista ampullaris morphology, abnormal ear development, abnormal endolymphatic duct morphology, abnormal hypothalamus secretion, abnormal inner ear canal fusion, abnormal kidney morphology, abnormal membranous labyrinth morphology, circling, decreased circulating growth hormone level, decreased vestibular hair cell number, head tilt, impaired balance, increased bone mineral content, nervous system phenotype, postnatal lethality, complete penetrance, small adenohypophysis, utricular degeneration, vestibular saccular degeneration [+]

Monarch Ortholog Phenotypes

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

Mouse (19 sources): abnormal bone mineralization, abnormal crista ampullaris morphology, abnormal ear development, abnormal endolymphatic duct morphology, abnormal hypothalamus secretion, abnormal inner ear canal fusion, abnormal kidney morphology, abnormal membranous labyrinth morphology, circling, decreased circulating growth hormone level, [+]