bhlhe22 Phenotypes

Phenotypes

XB-GENEPAGE-6457791

Gene Symbol: bhlhe22 Gene Name: basic helix-loop-helix family member e22

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: bhlhe22 assayed (11 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (20 sources): abnormal anterior corticospinal tract morphology, abnormal axon guidance, abnormal cerebral cortex morphology, abnormal chemical nociception, abnormal nervous system tract morphology, abnormal pyramidal decussation morphology, abnormal retina cone bipolar cell morphology, abnormal sensory capabilities/reflexes/nociception, abnormal somatosensory cortex morphology, absent anterior commissure, absent hippocampal commissure, behavior/neurological phenotype, decreased amacrine cell number, decreased brain size, decreased retina inner nuclear layer thickness, disorganized barrel cortex, excessive scratching, integument phenotype, nervous system phenotype, skin lesions [+]

Monarch Ortholog Phenotypes

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

Mouse (20 sources): abnormal anterior corticospinal tract morphology, abnormal axon guidance, abnormal cerebral cortex morphology, abnormal chemical nociception, abnormal nervous system tract morphology, abnormal pyramidal decussation morphology, abnormal retina cone bipolar cell morphology, abnormal sensory capabilities/reflexes/nociception, abnormal somatosensory cortex morphology, absent anterior commissure, [+]