rapidly progressive Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003678
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32 genes associated with the rapidly progressive phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARHGDIA Rho GDP dissociation inhibitor (GDI) alpha
ATP13A2 ATPase type 13A2
BAG3 BCL2-associated athanogene 3
C9ORF72 chromosome 9 open reading frame 72
CHMP2B charged multivesicular body protein 2B
COQ6 coenzyme Q6 monooxygenase
CRYAB crystallin, alpha B
CSF1R colony stimulating factor 1 receptor
DCTN1 dynactin 1
DNAJC5 DnaJ (Hsp40) homolog, subfamily C, member 5
DNAJC6 DnaJ (Hsp40) homolog, subfamily C, member 6
DYSF dysferlin
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
FHL1 four and a half LIM domains 1
GDAP1 ganglioside induced differentiation associated protein 1
GRN granulin
MFSD8 major facilitator superfamily domain containing 8
NHLRC1 NHL repeat containing E3 ubiquitin protein ligase 1
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
NPHS2 nephrosis 2, idiopathic, steroid-resistant (podocin)
PANK2 pantothenate kinase 2
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
PLEC plectin
PLEKHG5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5
POLG polymerase (DNA directed), gamma
PRNP prion protein
PSEN1 presenilin 1
SCARB2 scavenger receptor class B, member 2
SFTPB surfactant protein B
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
SNCA synuclein, alpha (non A4 component of amyloid precursor)
TARDBP TAR DNA binding protein