abnormal 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 nervous system tissue to regenerate following injury or disease (Mammalian Phenotype Ontology, MP_0004858)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004858
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Genes

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

Symbol Name
AVIL advillin
C3 complement component 3
CD36 CD36 molecule (thrombospondin receptor)
FOLH1 folate hydrolase (prostate-specific membrane antigen) 1
GAL galanin/GMAP prepropeptide
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
PTPRS protein tyrosine phosphatase, receptor type, S
RTN4 reticulon 4
RTN4R reticulon 4 receptor
SCYL1 SCY1-like 1 (S. cerevisiae)
SERPINE2 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 2
ST8SIA1 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B
Funding