hydranencephaly Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

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

Symbol Name Standardized Value
FLVCR2 feline leukemia virus subgroup C cellular receptor family, member 2 2.11291
ETV2 ets variant 2 1.6368
KDELR1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 1.39477
SLURP1 secreted LY6/PLAUR domain containing 1 1.0816
ZMYND10 zinc finger, MYND-type containing 10 1.0732
STXBP1 syntaxin binding protein 1 1.06774
MDM4 MDM4, p53 regulator 0.980531
CDK11A cyclin-dependent kinase 11A 0.951187
SPSB1 splA/ryanodine receptor domain and SOCS box containing 1 0.943274
COL4A1 collagen, type IV, alpha 1 0.939119
FKTN fukutin 0.680697
NDUFS4 NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase) 0.659215
CSH1 chorionic somatomammotropin hormone 1 (placental lactogen) 0.622575
CSH2 chorionic somatomammotropin hormone 2 0.60147
FLNA filamin A, alpha 0.493885
FGFR3 fibroblast growth factor receptor 3 0.425139
MDM2 MDM2 proto-oncogene, E3 ubiquitin protein ligase 0.289027
F5 coagulation factor V (proaccelerin, labile factor) 0.192971
ENO2 enolase 2 (gamma, neuronal) 0.184424
NPPA natriuretic peptide A 0.184128
CD68 CD68 molecule 0.163938