abnormal cerebellum vermis lobule morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the region of a cerebellar lobule that resides in the central section of the cerebellum between the two hemispheres; in humans, vermis lobule regions may be nearly continuous with the cerebellar hemisphere lobules dorsally but are separated by deeper longitudinal fissues in the ventral regions; in mammals, the vermis portion of the cerebellum has a foliation pattern along the AP axis that is distinct from the lateral cerebellar hemispheres (Mammalian Phenotype Ontology, MP_0009957)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009957
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6 gene mutations causing the abnormal cerebellum vermis lobule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARCN1 archain 1
EN2 engrailed homeobox 2
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
MID1 midline 1
MSX2 msh homeobox 2
UNC5C unc-5 homolog C (C. elegans)