dissociative disorder Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A disease of mental health in which the normally well-integrated functions of memory, identity, perception, or consciousness are separated (dissociated). (Human Disease Ontology, DOID_10935)
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Genes

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

Symbol Name Standardized Value
TRIM39 tripartite motif containing 39 1.59519
PDLIM4 PDZ and LIM domain 4 1.41271
FLVCR2 feline leukemia virus subgroup C cellular receptor family, member 2 1.20569
ADSS adenylosuccinate synthase 1.09167
TDG thymine-DNA glycosylase 1.07614
PAF1 Paf1, RNA polymerase II associated factor, homolog (S. cerevisiae) 1.04504
PEG10 paternally expressed 10 1.01891
MGAM maltase-glucoamylase 0.985164
OMG oligodendrocyte myelin glycoprotein 0.948685
TARS threonyl-tRNA synthetase 0.896641
FLNA filamin A, alpha 0.858952
UNG uracil-DNA glycosylase 0.855677
BCL3 B-cell CLL/lymphoma 3 0.847898
PITX1 paired-like homeodomain 1 0.783936
WDFY2 WD repeat and FYVE domain containing 2 0.640251
PFKM phosphofructokinase, muscle 0.568775
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B 0.565277
RELA v-rel avian reticuloendotheliosis viral oncogene homolog A 0.547032
PER2 period circadian clock 2 0.50459
PDYN prodynorphin 0.482084
APOLD1 apolipoprotein L domain containing 1 0.458241
PER1 period circadian clock 1 0.443171
PTPN12 protein tyrosine phosphatase, non-receptor type 12 0.439786
PTPRD protein tyrosine phosphatase, receptor type, D 0.433021
PTPN11 protein tyrosine phosphatase, non-receptor type 11 0.305948
BCL2L1 BCL2-like 1 0.212271
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