accessory spleen Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An accessory spleen is a round, iso-echogenic, homogenic and smooth structure and is seen as a normal variant mostly on the medial contour of the spleen, near the hilus or around the lower pole. This has no pathogenic relevance. (Human Phenotype Ontology, HP_0001747)
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6 gene mutations causing the accessory spleen phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CEP290 centrosomal protein 290kDa
CFC1 cripto, FRL-1, cryptic family 1
DNAH11 dynein, axonemal, heavy chain 11
LEFTY2 left-right determination factor 2
MEGF8 multiple EGF-like-domains 8
MKS1 Meckel syndrome, type 1