renal agenesis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000104
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Genes

39 genes associated with the renal agenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANOS1 anosmin 1
ATRX alpha thalassemia/mental retardation syndrome X-linked
CHD7 chromodomain helicase DNA binding protein 7
DHCR7 7-dehydrocholesterol reductase
EYA1 EYA transcriptional coactivator and phosphatase 1
FANCA Fanconi anemia, complementation group A
FANCB Fanconi anemia, complementation group B
FANCC Fanconi anemia, complementation group C
FANCD2 Fanconi anemia, complementation group D2
FANCE Fanconi anemia, complementation group E
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GDF6 growth differentiation factor 6
HNF1B HNF1 homeobox B
HOXD13 homeobox D13
INSL3 insulin-like 3 (Leydig cell)
ITGA8 integrin, alpha 8
KCTD1 potassium channel tetramerization domain containing 1
LRP4 low density lipoprotein receptor-related protein 4
MBTPS2 membrane-bound transcription factor peptidase, site 2
MKS1 Meckel syndrome, type 1
PAX2 paired box 2
PHGDH phosphoglycerate dehydrogenase
PROKR2 prokineticin receptor 2
PTPN11 protein tyrosine phosphatase, non-receptor type 11
PUF60 poly-U binding splicing factor 60KDa
RET ret proto-oncogene
RPL26 ribosomal protein L26
RXFP2 relaxin/insulin-like family peptide receptor 2
SALL4 spalt-like transcription factor 4
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SF3B4 splicing factor 3b, subunit 4, 49kDa
TBC1D24 TBC1 domain family, member 24
TBX1 T-box 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TP63 tumor protein p63
WNT3 wingless-type MMTV integration site family, member 3
WNT4 wingless-type MMTV integration site family, member 4