abnormal antigen presentation via mhc class i Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the process by which peptide, bound to major histocompatibility complex class I, is presented to lymphocytes at the surface of antigen presenting cells (Mammalian Phenotype Ontology, MP_0001836)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001836
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Genes

13 gene mutations causing the abnormal antigen presentation via mhc class i phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
B2M beta-2-microglobulin
ERAP1 endoplasmic reticulum aminopeptidase 1
NUP98 nucleoporin 98kDa
PRKDC protein kinase, DNA-activated, catalytic polypeptide
PSMB8 proteasome (prosome, macropain) subunit, beta type, 8
PSME2 proteasome (prosome, macropain) activator subunit 2 (PA28 beta)
STAT1 signal transducer and activator of transcription 1, 91kDa
STAT2 signal transducer and activator of transcription 2, 113kDa
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)
TAP2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)
TAPBP TAP binding protein (tapasin)
TPP2 tripeptidyl peptidase II
UNC93B1 unc-93 homolog B1 (C. elegans)