Familial Hematuria Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1305904
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
ACTN4 actinin, alpha 4
APOL1 apolipoprotein L, 1
CD2AP CD2-associated protein
CFHR5 complement factor H-related 5
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
COL4A4 collagen, type IV, alpha 4
COL4A5 collagen, type IV, alpha 5
FN1 fibronectin 1
INF2 inverted formin, FH2 and WH2 domain containing
ITGB4 integrin, beta 4
LAMA5 laminin, alpha 5
LAMB2 laminin, beta 2 (laminin S)
LAMB3 laminin, beta 3
LMX1B LIM homeobox transcription factor 1, beta
MYH9 myosin, heavy chain 9, non-muscle
NPHS2 nephrosis 2, idiopathic, steroid-resistant (podocin)
PDSS2 prenyl (decaprenyl) diphosphate synthase, subunit 2
PLCL1 phospholipase C-like 1
SCARB2 scavenger receptor class B, member 2
SMARCAL1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
TRPC6 transient receptor potential cation channel, subfamily C, member 6
WT1 Wilms tumor 1