mesangial abnormality Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the mesangium, i.e., of the central part of the renal glomerulus between capillaries. (Human Phenotype Ontology, HP_0001966)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001966
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Genes

8 genes associated with the mesangial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADA adenosine deaminase
APOE apolipoprotein E
ARHGDIA Rho GDP dissociation inhibitor (GDI) alpha
COQ6 coenzyme Q6 monooxygenase
LAMB2 laminin, beta 2 (laminin S)
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
PLCE1 phospholipase C, epsilon 1
WT1 Wilms tumor 1