cystic liver disease Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006706
Similar Terms
Downloads & Tools

Genes

20 genes associated with the cystic liver disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B9D1 B9 protein domain 1
B9D2 B9 protein domain 2
CC2D2A coiled-coil and C2 domain containing 2A
CEP290 centrosomal protein 290kDa
IFT122 intraflagellar transport 122
LRP5 low density lipoprotein receptor-related protein 5
MKS1 Meckel syndrome, type 1
NPHP3 nephronophthisis 3 (adolescent)
OFD1 oral-facial-digital syndrome 1
PKD1 polycystic kidney disease 1 (autosomal dominant)
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
PRKCSH protein kinase C substrate 80K-H
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
RPGRIP1L RPGRIP1-like
SEC63 SEC63 homolog (S. cerevisiae)
TCTN2 tectonic family member 2
TMEM216 transmembrane protein 216
TMEM231 transmembrane protein 231
TMEM67 transmembrane protein 67
WDPCP WD repeat containing planar cell polarity effector