abnormal albumin level Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Deviation from normal concentration of albumin in the blood. (Human Phenotype Ontology, HP_0012116)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012116
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Genes

20 genes associated with the abnormal albumin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTN4 actinin, alpha 4
ADCK4 aarF domain containing kinase 4
APTX aprataxin
ARHGDIA Rho GDP dissociation inhibitor (GDI) alpha
B2M beta-2-microglobulin
BMPR1A bone morphogenetic protein receptor, type IA
CCBE1 collagen and calcium binding EGF domains 1
DGAT1 diacylglycerol O-acyltransferase 1
DGUOK deoxyguanosine kinase
MPI mannose phosphate isomerase
MYO1E myosin IE
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
NPHS2 nephrosis 2, idiopathic, steroid-resistant (podocin)
PLCE1 phospholipase C, epsilon 1
PMM2 phosphomannomutase 2
PRF1 perforin 1 (pore forming protein)
PTPRO protein tyrosine phosphatase, receptor type, O
SAR1B secretion associated, Ras related GTPase 1B
SMAD4 SMAD family member 4
TTC37 tetratricopeptide repeat domain 37