meckel diverticulum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_9487)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002245
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Genes

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

Symbol Name
BRCA2 breast cancer 2, early onset
BRIP1 BRCA1 interacting protein C-terminal helicase 1
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
FGFR1 fibroblast growth factor receptor 1
FOXF1 forkhead box F1
GPC3 glypican 3
PALB2 partner and localizer of BRCA2
RAD51C RAD51 paralog C
RBM8A RNA binding motif protein 8A
SLX4 SLX4 structure-specific endonuclease subunit