pou4f1 Phenotypes

Phenotypes

XB-GENEPAGE-853138

Gene Symbol: pou4f1 Gene Name: POU class 4 homeobox 1

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.
Manual annotations: pou4f1 assayed (4 sources)
Computed annotations: pou4f1 assayed (6 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (22 sources): abnormal cranial ganglia morphology, abnormal dorsal root ganglion morphology, abnormal epithalamus morphology, abnormal inferior olivary complex morphology, abnormal medulla oblongata morphology, abnormal red nucleus morphology, abnormal retina ganglion cell morphology, abnormal trigeminal ganglion morphology, abnormal vestibular ganglion morphology, absent gastric milk in neonates, absent red nucleus, absent suckling reflex, aphagia, cochlear ganglion hypoplasia, impaired righting response, neonatal lethality, complete penetrance, no abnormal phenotype detected, perinatal lethality, complete penetrance, small dorsal root ganglion, small geniculate ganglion, small trigeminal ganglion, vision/eye phenotype [+]

Monarch Ortholog Phenotypes

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

Mouse (22 sources): abnormal cranial ganglia morphology, abnormal dorsal root ganglion morphology, abnormal epithalamus morphology, abnormal inferior olivary complex morphology, abnormal medulla oblongata morphology, abnormal red nucleus morphology, abnormal retina ganglion cell morphology, abnormal trigeminal ganglion morphology, abnormal vestibular ganglion morphology, absent gastric milk in neonates, [+]