Abnormal Renal Morphology Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Any structural anomaly of the kidney. (Human Phenotype Ontology, HP_0012210)
External Link https://www.disgenet.org/browser/0/1/0/C4551596
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Genes

35 genes associated with the disease Abnormal Renal Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADGRG2 adhesion G protein-coupled receptor G2
AFP alpha-fetoprotein
BEST1 bestrophin 1
CEP19 centrosomal protein 19kDa
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
DGCR8 DGCR8 microprocessor complex subunit
DLK1 delta-like 1 homolog (Drosophila)
DMD dystrophin
EYA1 EYA transcriptional coactivator and phosphatase 1
FBN1 fibrillin 1
FGFR2 fibroblast growth factor receptor 2
FLCN folliculin
GLMN glomulin, FKBP associated protein
GREB1L growth regulation by estrogen in breast cancer-like
HDGF hepatoma-derived growth factor
HNF1B HNF1 homeobox B
IRF6 interferon regulatory factor 6
LHX1 LIM homeobox 1
LRP4 low density lipoprotein receptor-related protein 4
MIP major intrinsic protein of lens fiber
PACS1 phosphofurin acidic cluster sorting protein 1
PAH phenylalanine hydroxylase
PAX2 paired box 2
PBX1 pre-B-cell leukemia homeobox 1
PIGV phosphatidylinositol glycan anchor biosynthesis, class V
PIGX phosphatidylinositol glycan anchor biosynthesis, class X
POMC proopiomelanocortin
POR P450 (cytochrome) oxidoreductase
RAI1 retinoic acid induced 1
SIX1 SIX homeobox 1
SLC35A2 solute carrier family 35 (UDP-galactose transporter), member A2
SLIT3 slit homolog 3 (Drosophila)
SMARCAL1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
TFAP2B transcription factor AP-2 beta (activating enhancer binding protein 2 beta)
TGFB1 transforming growth factor, beta 1