tethered spinal cord syndrome 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_1089)
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20 genes co-occuring with the disease tethered spinal cord syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ITFG1 integrin alpha FG-GAP repeat containing 1 2.00378
NKX2-8 NK2 homeobox 8 1.57111
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family) 1.30532
MNX1 motor neuron and pancreas homeobox 1 1.18367
CHST14 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14 1.0265
CYS1 cystin 1 1.02313
HOXA1 homeobox A1 0.97338
PEPD peptidase D 0.901567
NCOA1 nuclear receptor coactivator 1 0.824128
HSF4 heat shock transcription factor 4 0.790492
APOLD1 apolipoprotein L domain containing 1 0.546256
HMGA2 high mobility group AT-hook 2 0.544705
CAMP cathelicidin antimicrobial peptide 0.541217
ATP12A ATPase, H+/K+ transporting, nongastric, alpha polypeptide 0.526518
ATP4A ATPase, H+/K+ exchanging, alpha polypeptide 0.526132
FGFR2 fibroblast growth factor receptor 2 0.42589
CST3 cystatin C 0.40904
AFP alpha-fetoprotein 0.392629
IMMT inner membrane protein, mitochondrial 0.343473
ACHE acetylcholinesterase (Yt blood group) 0.189551