Congenital Absence Of Kidney Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0542519
Similar Terms
Downloads & Tools

Genes

30 genes associated with the disease Congenital Absence Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AFP alpha-fetoprotein
ANOS1 anosmin 1
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
DDX3X DEAD (Asp-Glu-Ala-Asp) box helicase 3, X-linked
FGFR1 fibroblast growth factor receptor 1
FRAS1 Fraser extracellular matrix complex subunit 1
FREM1 FRAS1 related extracellular matrix 1
FREM2 FRAS1 related extracellular matrix protein 2
GDNF glial cell derived neurotrophic factor
GEN1 GEN1 Holliday junction 5' flap endonuclease
GGT1 gamma-glutamyltransferase 1
GGTLC3 gamma-glutamyltransferase light chain 3
GREB1L growth regulation by estrogen in breast cancer-like
HNF1A HNF1 homeobox A
HNF1B HNF1 homeobox B
HOXD11 homeobox D11
IFNG interferon, gamma
IFT27 intraflagellar transport 27
IRF6 interferon regulatory factor 6
NOTUM notum pectinacetylesterase homolog (Drosophila)
PAX2 paired box 2
PUF60 poly-U binding splicing factor 60KDa
RAB40B RAB40B, member RAS oncogene family
RARA retinoic acid receptor, alpha
RET ret proto-oncogene
SERPINA4 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 4
SIX1 SIX homeobox 1
SOX8 SRY (sex determining region Y)-box 8
SOX9 SRY (sex determining region Y)-box 9
TMCO1 transmembrane and coiled-coil domains 1