abnormal peripheral nervous system regeneration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description changes in the ability or inability of healthy peripheral nervous system tissue to regenerate following injury or disease (Mammalian Phenotype Ontology, MP_0004220)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004220
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Genes

11 gene mutations causing the abnormal peripheral nervous system regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
C3 complement component 3
CD36 CD36 molecule (thrombospondin receptor)
FOLH1 folate hydrolase (prostate-specific membrane antigen) 1
LARGE like-glycosyltransferase
NGFR nerve growth factor receptor
NOS1 nitric oxide synthase 1 (neuronal)
NOS2 nitric oxide synthase 2, inducible
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
PTPRF protein tyrosine phosphatase, receptor type, F
SCYL1 SCY1-like 1 (S. cerevisiae)
SERPINE2 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 2