supernumerary spleens Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of two or more accessory spleens. (Human Phenotype Ontology, HP_0009799)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009799
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Genes

10 genes associated with the supernumerary spleens phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CCDC39 coiled-coil domain containing 39
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
GDF1 growth differentiation factor 1
GPC3 glypican 3
HYLS1 hydrolethalus syndrome 1
MKS1 Meckel syndrome, type 1
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NPHP3 nephronophthisis 3 (adolescent)
RAB23 RAB23, member RAS oncogene family
ZIC3 Zic family member 3