gamma heavy chain disease Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A heavy chain disease that results from an overproduction of gamma antibody (IgG). (Human Disease Ontology, DOID_0060127)
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Genes

12 genes co-occuring with the disease gamma heavy chain disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SLC3A2 solute carrier family 3 (amino acid transporter heavy chain), member 2 1.7623
IGHV1-2 immunoglobulin heavy variable 1-2 1.27999
WARS tryptophanyl-tRNA synthetase 1.01132
PNMT phenylethanolamine N-methyltransferase 0.960797
GIF gastric intrinsic factor (vitamin B synthesis) 0.676308
MYD88 myeloid differentiation primary response 88 0.613965
FUT4 fucosyltransferase 4 (alpha (1,3) fucosyltransferase, myeloid-specific) 0.515725
CDR2 cerebellar degeneration-related protein 2, 62kDa 0.419517
CD79A CD79a molecule, immunoglobulin-associated alpha 0.339806
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog 0.238054
KRAS Kirsten rat sarcoma viral oncogene homolog 0.196459
HRAS Harvey rat sarcoma viral oncogene homolog 0.158778