pancreatic cysts Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A cyst of the pancreas that possess a lining of mucous epithelium. (Human Phenotype Ontology, HP_0001737)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001737
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Genes

18 genes associated with the pancreatic cysts 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
MKS1 Meckel syndrome, type 1
NPHP3 nephronophthisis 3 (adolescent)
OFD1 oral-facial-digital syndrome 1
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
RBM8A RNA binding motif protein 8A
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
RPGRIP1L RPGRIP1-like
TCTN2 tectonic family member 2
TMEM216 transmembrane protein 216
TMEM231 transmembrane protein 231
TMEM67 transmembrane protein 67
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
WDPCP WD repeat containing planar cell polarity effector
XPNPEP3 X-prolyl aminopeptidase 3, mitochondrial