hypoproteinemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A decreased concentration of protein in the blood. (Human Phenotype Ontology, HP_0003075)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003075
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Genes

11 genes associated with the hypoproteinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B2M beta-2-microglobulin
DCLRE1C DNA cross-link repair 1C
DPAGT1 dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase)
LAMB2 laminin, beta 2 (laminin S)
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
PRF1 perforin 1 (pore forming protein)
PRSS1 protease, serine, 1 (trypsin 1)
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2
TMPRSS15 transmembrane protease, serine 15
UBR1 ubiquitin protein ligase E3 component n-recognin 1