mhc class i deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0060009)
Similar Terms
Downloads & Tools

Genes

16 genes co-occuring with the disease mhc class i deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TAP2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) 1.87148
TAPBP TAP binding protein (tapasin) 1.42762
RPL34 ribosomal protein L34 1.34417
RFXAP regulatory factor X-associated protein 1.34068
RFX5 regulatory factor X, 5 (influences HLA class II expression) 1.14178
HLA-B major histocompatibility complex, class I, B 0.804436
KLRC1 killer cell lectin-like receptor subfamily C, member 1 0.799103
KLRD1 killer cell lectin-like receptor subfamily D, member 1 0.779432
RFXANK regulatory factor X-associated ankyrin-containing protein 0.765127
CXCL11 chemokine (C-X-C motif) ligand 11 0.673917
MICA MHC class I polypeptide-related sequence A 0.559839
CD40 CD40 molecule, TNF receptor superfamily member 5 0.53928
ANK1 ankyrin 1, erythrocytic 0.516494
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) 0.474498
CD80 CD80 molecule 0.267977
IL4 interleukin 4 0.162505