axonal loss Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A reduction in the number of axons in the peripheral nervous system. (Human Phenotype Ontology, HP_0003447)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003447
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Genes

8 genes associated with the axonal loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BAG3 BCL2-associated athanogene 3
FIG4 FIG4 phosphoinositide 5-phosphatase
INF2 inverted formin, FH2 and WH2 domain containing
MOCS1 molybdenum cofactor synthesis 1
MOCS2 molybdenum cofactor synthesis 2
NDRG1 N-myc downstream regulated 1
TREM2 triggering receptor expressed on myeloid cells 2
TYROBP TYRO protein tyrosine kinase binding protein