abnormal cerebellum posterior vermis morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the posterior portion of the narrow middle zone between the two hemispheres of the cerebellum that is located posterior to the primary fissure (Mammalian Phenotype Ontology, MP_0000869)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000869
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7 gene mutations causing the abnormal cerebellum posterior vermis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARCN1 archain 1
EN1 engrailed homeobox 1
EN2 engrailed homeobox 2
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
LMX1A LIM homeobox transcription factor 1, alpha
MSX2 msh homeobox 2
NPC1 Niemann-Pick disease, type C1