sun1 Phenotypes

Phenotypes

XB-GENEPAGE-995940

Gene Symbol: sun1 Gene Name: Sad1 and UNC84 domain containing 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.
Computed annotations: sun1 assayed (6 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (38 sources): abnormal cerebellar foliation, abnormal cerebellum development, abnormal cerebellum external granule cell layer morphology, abnormal chromosomal synapsis, abnormal cochlear outer hair cell morphology, abnormal contextual conditioning behavior, abnormal female meiosis, abnormal locomotor behavior, abnormal male meiosis, abnormal meiotic attachment of telomere to nuclear envelope, abnormal prepulse inhibition, abnormal Purkinje cell migration, abnormal Purkinje cell morphology, abnormal retina outer nuclear layer morphology, abnormal spermatocyte morphology, abnormal startle reflex, abnormal total retina thickness, abnormal vitreous body morphology, absent cerebellum fissure, absent oocytes, absent ovarian follicles, absent pinna reflex, arrest of male meiosis, cochlear outer hair cell degeneration, decreased brain weight, decreased male germ cell number, decreased prepulse inhibition, decreased startle reflex, decreased testis weight, decreased total retina thickness, ectopic Purkinje cell, increased or absent threshold for auditory brainstem response, increased ovary apoptosis, increased testis apoptosis, no abnormal phenotype detected, small cerebellum, small ovary, small superior vagus ganglion [+]

Monarch Ortholog Phenotypes

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

Mouse (38 sources): abnormal cerebellar foliation, abnormal cerebellum development, abnormal cerebellum external granule cell layer morphology, abnormal chromosomal synapsis, abnormal cochlear outer hair cell morphology, abnormal contextual conditioning behavior, abnormal female meiosis, abnormal locomotor behavior, abnormal male meiosis, abnormal meiotic attachment of telomere to nuclear envelope, [+]