stiff-person syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A movement disease that is of unknown etiology characterized by progressive rigidity. (Human Disease Ontology, DOID_13366)
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Genes

46 genes co-occuring with the disease stiff-person syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
GAD2 glutamate decarboxylase 2 (pancreatic islets and brain, 65kDa) 3.0943
AMPH amphiphysin 2.63463
GAD1 glutamate decarboxylase 1 (brain, 67kDa) 1.94689
GPHN gephyrin 1.69815
GABARAP GABA(A) receptor-associated protein 1.5194
NDUFB11 NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 11, 17.3kDa 0.96918
HOMER3 homer scaffolding protein 3 0.95996
MICA MHC class I polypeptide-related sequence A 0.91308
TRAK1 trafficking protein, kinesin binding 1 0.91061
DPYSL5 dihydropyrimidinase-like 5 0.88434
CSAD cysteine sulfinic acid decarboxylase 0.860999
MAG myelin associated glycoprotein 0.76921
KCNA6 potassium channel, voltage gated shaker related subfamily A, member 6 0.750457
SNAP91 synaptosomal-associated protein, 91kDa 0.690694
ALDH5A1 aldehyde dehydrogenase 5 family, member A1 0.679898
GLRA1 glycine receptor, alpha 1 0.677504
BIN1 bridging integrator 1 0.640645
AK5 adenylate kinase 5 0.634349
DPP6 dipeptidyl-peptidase 6 0.607323
PPT2 palmitoyl-protein thioesterase 2 0.555956
LAD1 ladinin 1 0.536957
CAMP cathelicidin antimicrobial peptide 0.512264
ANK3 ankyrin 3, node of Ranvier (ankyrin G) 0.512264
PNMA2 paraneoplastic Ma antigen 2 0.506507
KCNA2 potassium channel, voltage gated shaker related subfamily A, member 2 0.499231
NUDT10 nudix (nucleoside diphosphate linked moiety X)-type motif 10 0.495793
AKR7A2 aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) 0.444676
DDC dopa decarboxylase (aromatic L-amino acid decarboxylase) 0.418768
TPO thyroid peroxidase 0.406425
TTN titin 0.403064
WDR11 WD repeat domain 11 0.35082
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1 0.342372
HLA-DRB1 major histocompatibility complex, class II, DR beta 1 0.324823
CDR2 cerebellar degeneration-related protein 2, 62kDa 0.311377
ELAVL3 ELAV like neuron-specific RNA binding protein 3 0.309566
INS insulin 0.295851
CDR1 cerebellar degeneration-related protein 1, 34kDa 0.276158
RCVRN recoverin 0.269043
LGI1 leucine-rich, glioma inactivated 1 0.258417
CNTN2 contactin 2 (axonal) 0.249608
TH tyrosine hydroxylase 0.230755
OPA1 optic atrophy 1 (autosomal dominant) 0.225917
GRM1 glutamate receptor, metabotropic 1 0.185016
CLN3 ceroid-lipofuscinosis, neuronal 3 0.177029
HSPD1 heat shock 60kDa protein 1 (chaperonin) 0.175411
GCH1 GTP cyclohydrolase 1 0.168381