Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (2) GO Terms (11) Nucleotides (195) Proteins (80) Interactants (198) Wiki

katnb1     katanin regulatory subunit B1

Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (18 sources): Cognitive impairment, Global developmental delay, Gray matter heterotopia, Hyperreflexia, Hypoplasia of the corpus callosum, Limb hypertonia, Lissencephaly, Microcephaly, Microlissencephaly, Motor delay, [+]
Mouse (30 sources): abnormal cell morphology, abnormal cortical ventricular zone morphology, abnormal embryo morphology, abnormal erythropoiesis, abnormal male meiosis, abnormal manchette morphology, abnormal meiotic spindle morphology, abnormal mitosis, abnormal mitotic spindle morphology, abnormal neuronal precursor proliferation, [+]

View all ortholog results at Monarch