increased csf protein Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased concentration of protein in the cerebrospinal fluid. (Human Phenotype Ontology, HP_0002922)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002922
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Genes

17 genes associated with the increased csf protein phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARSA arylsulfatase A
CD59 CD59 molecule, complement regulatory protein
EGR2 early growth response 2
GALC galactosylceramidase
GFAP glial fibrillary acidic protein
MPZ myelin protein zero
OCLN occludin
PHYH phytanoyl-CoA 2-hydroxylase
PMP22 peripheral myelin protein 22
POLG polymerase (DNA directed), gamma
PRF1 perforin 1 (pore forming protein)
PRX periaxin
PSAP prosaposin
RANBP2 RAN binding protein 2
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SUMF1 sulfatase modifying factor 1
TTR transthyretin