abnormal spinal cord ventral horn morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the ventral grey column of the spinal cord (Mammalian Phenotype Ontology, MP_0005112)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005112
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12 gene mutations causing the abnormal spinal cord ventral horn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CDK5 cyclin-dependent kinase 5
CLN8 ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
DYNC1H1 dynein, cytoplasmic 1, heavy chain 1
EEF1A2 eukaryotic translation elongation factor 1 alpha 2
GLRB glycine receptor, beta
KIF1B kinesin family member 1B
OLIG2 oligodendrocyte lineage transcription factor 2
PITPNA phosphatidylinositol transfer protein, alpha
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
TTPA tocopherol (alpha) transfer protein
VEGFA vascular endothelial growth factor A