Finnish Congenital Nephrotic Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0403399
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Genes

10 genes associated with the disease Finnish Congenital Nephrotic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AFP alpha-fetoprotein
ALB albumin
ALG1 ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase
APLP1 amyloid beta (A4) precursor-like protein 1
CRB2 crumbs family member 2
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
NPHS2 nephrosis 2, idiopathic, steroid-resistant (podocin)
TREH trehalase (brush-border membrane glycoprotein)
TTC21B tetratricopeptide repeat domain 21B
TUBA1B tubulin, alpha 1b