absent liver Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the bile-secreting exocrine gland, which is important for detoxification; for fat, carbohydrate, and protein metabolism; and for glycogen storage (Mammalian Phenotype Ontology, MP_0011877)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011877
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3 gene mutations causing the absent liver phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
HHEX hematopoietically expressed homeobox
ICMT isoprenylcysteine carboxyl methyltransferase
NPM1 nucleophosmin (nucleolar phosphoprotein B23, numatrin)