striatonigral degeneration Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [LS]. (Human Disease Ontology, DOID_4751)
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27 genes co-occuring with the disease striatonigral degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TH tyrosine hydroxylase 1.31275
STRN striatin, calmodulin binding protein 1.2595
NUP62 nucleoporin 62kDa 1.18755
CALB1 calbindin 1, 28kDa 1.00879
RAB3A RAB3A, member RAS oncogene family 0.909376
TAC1 tachykinin, precursor 1 0.902389
REXO1L1P REX1, RNA exonuclease 1 homolog (S. cerevisiae)-like 1, pseudogene 0.782707
KIAA0101 KIAA0101 0.743141
MAP1B microtubule-associated protein 1B 0.732596
CAPN2 calpain 2, (m/II) large subunit 0.709975
CSF2RA colony stimulating factor 2 receptor, alpha, low-affinity (granulocyte-macrophage) 0.70434
SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1 0.680297
MAP2 microtubule-associated protein 2 0.663578
FOSB FBJ murine osteosarcoma viral oncogene homolog B 0.633169
GYPE glycophorin E (MNS blood group) 0.626888
CYLD cylindromatosis (turban tumor syndrome) 0.626495
DDC dopa decarboxylase (aromatic L-amino acid decarboxylase) 0.612401
PENK proenkephalin 0.579661
TPH1 tryptophan hydroxylase 1 0.503824
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B 0.418019
CRYAB crystallin, alpha B 0.412779
VIM vimentin 0.392257
PTER phosphotriesterase related 0.358183
ATXN3 ataxin 3 0.354499
PTPRC protein tyrosine phosphatase, receptor type, C 0.353395
DRD2 dopamine receptor D2 0.252422
GDNF glial cell derived neurotrophic factor 0.232836