abnormal corticospinal tract morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the corticospinal fibers that arise from the pyramidal cells within the cerebral cortex layer V of the precentral motor area, the premotor area and the postcentral gyrus, then descend into and through the medulla to form the lateral corticospinal tract and the anterior corticospinal tract (Mammalian Phenotype Ontology, MP_0002878)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002878
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12 gene mutations causing the abnormal corticospinal tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
BHLHE22 basic helix-loop-helix family, member e22
CELSR3 cadherin, EGF LAG seven-pass G-type receptor 3
CHN1 chimerin 1
DCC DCC netrin 1 receptor
EFNB3 ephrin-B3
EPHA4 EPH receptor A4
HSPD1 heat shock 60kDa protein 1 (chaperonin)
L1CAM L1 cell adhesion molecule
NMNAT2 nicotinamide nucleotide adenylyltransferase 2
NTN1 netrin 1
UNC5C unc-5 homolog C (C. elegans)