abnormality of the gastric mucosa Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the gastric mucous membrane. (Human Phenotype Ontology, HP_0004295)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004295
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Genes

32 genes associated with the abnormality of the gastric mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC2 ATP-binding cassette, sub-family C (CFTR/MRP), member 2
AIRE autoimmune regulator
BAZ1B bromodomain adjacent to zinc finger domain, 1B
BIRC3 baculoviral IAP repeat containing 3
CDH1 cadherin 1, type 1, E-cadherin (epithelial)
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1)
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CDKN2B cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)
CDKN2C cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4)
CISD2 CDGSH iron sulfur domain 2
CLIP2 CAP-GLY domain containing linker protein 2
DSP desmoplakin
ELN elastin
FERMT1 fermitin family member 1
FOXP1 forkhead box P1
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD)
JUP junction plakoglobin
KIAA2022 KIAA2022
KRAS Kirsten rat sarcoma viral oncogene homolog
LBR lamin B receptor
LIMK1 LIM domain kinase 1
LRBA LPS-responsive vesicle trafficking, beach and anchor containing
MALT1 MALT1 paracaspase
MEN1 multiple endocrine neoplasia I
RFC2 replication factor C (activator 1) 2, 40kDa
SLCO1B1 solute carrier organic anion transporter family, member 1B1
SLCO1B3 solute carrier organic anion transporter family, member 1B3
SLCO2A1 solute carrier organic anion transporter family, member 2A1
TBL2 transducin (beta)-like 2
WFS1 Wolfram syndrome 1 (wolframin)