pou3f3 Phenotypes

Phenotypes

XB-GENEPAGE-920671

Gene Symbol: pou3f3 Gene Name: POU class 3 homeobox 3

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: pou3f3 assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (20 sources): abnormal cerebral cortex morphology, abnormal distal convoluted tubule morphology, abnormal incus short process morphology, abnormal loop of Henle morphology, abnormal renal tubule morphology, abnormal styloid process morphology, absent temporal bone squamous part, absent temporomandibular joint, absent zygomatic bone, decreased circulating glucose level, decreased kidney cell proliferation, decreased kidney weight, decreased urine sodium level, delayed kidney development, increased circulating creatinine level, increased kidney apoptosis, neonatal lethality, complete penetrance, renal/urinary system phenotype, small kidney, truncated loop of Henle [+]

Monarch Ortholog Phenotypes

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

Mouse (20 sources): abnormal cerebral cortex morphology, abnormal distal convoluted tubule morphology, abnormal incus short process morphology, abnormal loop of Henle morphology, abnormal renal tubule morphology, abnormal styloid process morphology, absent temporal bone squamous part, absent temporomandibular joint, absent zygomatic bone, decreased circulating glucose level, [+]