abnormality of the astrocytes Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of astrocytes. (Human Phenotype Ontology, HP_0100707)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100707
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Genes

11 genes associated with the abnormality of the astrocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APC adenomatous polyposis coli
CDKN2A cyclin-dependent kinase inhibitor 2A
ERBB2 erb-b2 receptor tyrosine kinase 2
MLH1 mutL homolog 1
MSH2 mutS homolog 2
MSH6 mutS homolog 6
NF1 neurofibromin 1
NF2 neurofibromin 2 (merlin)
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2