septin9 Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (293)

Interactants (35)

XB-GENEPAGE-1012201

Gene Symbol: septin9 Gene Name: septin 9

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: septin9 assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (19 sources): Axonal degeneration, Blepharophimosis, Brachial plexus neuropathy, Cleft palate, Deeply set eye, Depressed nasal bridge, Epicanthus, Facial asymmetry, Hyporeflexia, Hypotelorism, Low-set ears, Muscle weakness, Narrow mouth, Peripheral axonal degeneration, Peripheral neuropathy, Ptosis, Short stature, Skeletal muscle atrophy, Upslanted palpebral fissure [+]
Mouse (14 sources): abnormal T cell differentiation, decreased CD4-positive, alpha beta T cell number, decreased CD4-positive, alpha-beta memory T cell number, decreased CD8-positive, alpha-beta memory T cell number, decreased DN4 thymocyte number, decreased T cell proliferation, decreased regulatory T cell number, decreased single-positive T cell number, embryonic lethality during organogenesis, complete penetrance, increased CD8-positive, alpha-beta memory T cell number, increased DN3 thymocyte number, increased apoptosis, increased double-negative T cell number, no abnormal phenotype detected [+]
View all ortholog results at Monarch