Hypoproteinemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A decreased concentration of protein in the blood. (Human Phenotype Ontology, HP_0003075)
External Link https://www.disgenet.org/browser/0/1/0/C0020639
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Genes

24 genes associated with the disease Hypoproteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACADVL acyl-CoA dehydrogenase, very long chain
ALB albumin
ANGPTL3 angiopoietin-like 3
APOA1 apolipoprotein A-I
ARID5B AT rich interactive domain 5B (MRF1-like)
B2M beta-2-microglobulin
BTBD8 BTB (POZ) domain containing 8
CD55 CD55 molecule, decay accelerating factor for complement (Cromer blood group)
DCLRE1C DNA cross-link repair 1C
LAMB2 laminin, beta 2 (laminin S)
LIPC lipase, hepatic
MTX1 metaxin 1
NEB nebulin
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
RPS6KB1 ribosomal protein S6 kinase, 70kDa, polypeptide 1
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13
SLC9A6 solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
SMAD4 SMAD family member 4
TMPRSS15 transmembrane protease, serine 15
UBR1 ubiquitin protein ligase E3 component n-recognin 1