mutism Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A speech disorder that involves a complete inability to speak. (Human Disease Ontology, DOID_4189)
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Genes

26 genes co-occuring with the disease mutism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ACOX3 acyl-CoA oxidase 3, pristanoyl 1.52468
FANCL Fanconi anemia, complementation group L 1.19445
POLD1 polymerase (DNA directed), delta 1, catalytic subunit 1.11141
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide 1.08915
HIF3A hypoxia inducible factor 3, alpha subunit 1.04167
DRD5 dopamine receptor D5 0.987271
TXNDC9 thioredoxin domain containing 9 0.978426
SH2B3 SH2B adaptor protein 3 0.872462
QDPR quinoid dihydropteridine reductase 0.861818
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like 0.758601
MAPT microtubule-associated protein tau 0.717232
PNMA2 paraneoplastic Ma antigen 2 0.66596
GAD2 glutamate decarboxylase 2 (pancreatic islets and brain, 65kDa) 0.620226
CP ceruloplasmin (ferroxidase) 0.6003
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2 0.591337
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled 0.546644
MGP matrix Gla protein 0.400453
CBS cystathionine-beta-synthase 0.383708
CABIN1 calcineurin binding protein 1 0.379626
PIK3C2A phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha 0.265494
PSEN1 presenilin 1 0.258064
GFAP glial fibrillary acidic protein 0.238403
MB myoglobin 0.224196
AVP arginine vasopressin 0.198386
SYP synaptophysin 0.174881
TRH thyrotropin-releasing hormone 0.162908