abnormal level of surface class i molecules Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the normal concentration of major histocompatibility complex class I molecules expressed at the cell surface (Mammalian Phenotype Ontology, MP_0001839)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001839
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Genes

11 gene mutations causing the abnormal level of surface class i molecules 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
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