Tubulointerstitial Abnormality Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality that involves the tubules and interstitial tissue of the kidney. (Human Phenotype Ontology, HP_0001969)
External Link https://www.disgenet.org/browser/0/1/0/C4025732
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Genes

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

Symbol Name
BAZ1B bromodomain adjacent to zinc finger domain, 1B
CLIP2 CAP-GLY domain containing linker protein 2
COX1
COX2
COX3
CTNS cystinosin, lysosomal cystine transporter
ELN elastin
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
LIMK1 LIM domain kinase 1
MT-ND4 NADH dehydrogenase, subunit 4 (complex I)
MT-ND5 NADH dehydrogenase, subunit 5 (complex I)
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
ND1
RFC2 replication factor C (activator 1) 2, 40kDa
TBL2 transducin (beta)-like 2