abnormal lamina terminalis morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the anterior-most (rostral) portion of the wall of the neural tube, formed by closure of the anterior neuropore; the median strip of the anterior wall of the prosencephalon, which persists in a relatively unchanged state as the cerebral hemispheres grow out forward beyond the original anterior end of the prosencephalon; in the developed brain, the lamina terminalis remains as the thin rostral wall of the third ventricle, stretching from the bases of the major cerebral commissures (the anterior commissure, the commissure of the fornix, and the rostrum of the corpus callosum) to the dorsal surface of the optic chiasm (Mammalian Phenotype Ontology, MP_0012540)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012540
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Genes

3 gene mutations causing the abnormal lamina terminalis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CASP9 caspase 9, apoptosis-related cysteine peptidase
CDON cell adhesion associated, oncogene regulated
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein