ift56 Phenotypes

Phenotypes

XB-GENEPAGE-1002213

Gene Symbol: ift56 Gene Name: intraflagellar transport 56

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: ift56 assayed (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (21 sources): abnormal Sertoli cell morphology, abnormal bony labyrinth, abnormal developmental patterning, abnormal male meiosis, abnormal manchette morphology, abnormal motile primary cilium morphology, abnormal neuron specification, abnormal photoreceptor outer segment morphology, abnormal sperm flagellum morphology, abnormal spermatid morphology, abnormal spermiogenesis, absent sperm flagellum, decreased body size, decreased total retina thickness, impaired swimming, increased or absent threshold for auditory brainstem response, postnatal lethality, incomplete penetrance, premature death, prenatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, renal/urinary system phenotype [+]

Monarch Ortholog Phenotypes

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

Mouse (21 sources): abnormal Sertoli cell morphology, abnormal bony labyrinth, abnormal developmental patterning, abnormal male meiosis, abnormal manchette morphology, abnormal motile primary cilium morphology, abnormal neuron specification, abnormal photoreceptor outer segment morphology, abnormal sperm flagellum morphology, abnormal spermatid morphology, [+]