genital tract atresia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Congenital occlusion of a tube in the genital tract. (Human Phenotype Ontology, HP_0001827)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001827
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Genes

26 genes associated with the genital tract atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARL6 ADP-ribosylation factor-like 6
BBS1 Bardet-Biedl syndrome 1
BBS10 Bardet-Biedl syndrome 10
BBS12 Bardet-Biedl syndrome 12
BBS2 Bardet-Biedl syndrome 2
BBS4 Bardet-Biedl syndrome 4
BBS5 Bardet-Biedl syndrome 5
BBS7 Bardet-Biedl syndrome 7
BBS9 Bardet-Biedl syndrome 9
CEP290 centrosomal protein 290kDa
FGFR2 fibroblast growth factor receptor 2
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1
IFT27 intraflagellar transport 27
ITGA8 integrin, alpha 8
LZTFL1 leucine zipper transcription factor-like 1
MKKS McKusick-Kaufman syndrome
MKS1 Meckel syndrome, type 1
NEK1 NIMA-related kinase 1
PAX2 paired box 2
RET ret proto-oncogene
TRIM32 tripartite motif containing 32
TTC8 tetratricopeptide repeat domain 8
WDPCP WD repeat containing planar cell polarity effector
WNT3 wingless-type MMTV integration site family, member 3