duodenal stenosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The narrowing or partial blockage of a portion of the duodenum. (Human Phenotype Ontology, HP_0100867)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100867
Similar Terms
Downloads & Tools

Genes

31 genes associated with the duodenal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTG2 actin, gamma 2, smooth muscle, enteric
BRCA2 breast cancer 2, early onset
BRIP1 BRCA1 interacting protein C-terminal helicase 1
BUB1 BUB1 mitotic checkpoint serine/threonine kinase
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
BUB3 BUB3 mitotic checkpoint protein
CEP57 centrosomal protein 57kDa
ERCC4 excision repair cross-complementation group 4
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
FANCF Fanconi anemia, complementation group F
FANCG Fanconi anemia, complementation group G
FANCI Fanconi anemia, complementation group I
FANCL Fanconi anemia, complementation group L
FANCM Fanconi anemia, complementation group M
FBN2 fibrillin 2
FOXF1 forkhead box F1
GATA1 GATA binding protein 1 (globin transcription factor 1)
ITGA6 integrin, alpha 6
ITGB4 integrin, beta 4
PALB2 partner and localizer of BRCA2
PORCN porcupine homolog (Drosophila)
RAD51C RAD51 paralog C
RARB retinoic acid receptor, beta
SHH sonic hedgehog
SLX4 SLX4 structure-specific endonuclease subunit
STRA6 stimulated by retinoic acid 6
TTC7A tetratricopeptide repeat domain 7A