annular pancreas Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A congenital anomaly in which the pancreas completely (or sometimes incompletely) encircles the second portion of duodenum and occasionally obstructs the more proximal duodenum. (Human Phenotype Ontology, HP_0001734)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001734
Similar Terms
Downloads & Tools

Genes

9 genes associated with the annular pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FOXF1 forkhead box F1
GABRD gamma-aminobutyric acid (GABA) A receptor, delta
KCNAB2 potassium channel, voltage gated subfamily A regulatory beta subunit 2
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
PRDM16 PR domain containing 16
RARB retinoic acid receptor, beta
RECQL4 RecQ protein-like 4
SKI SKI proto-oncogene
STRA6 stimulated by retinoic acid 6