pancreatic acinar hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size of the secretory units of the exocrine pancreas, where fluid containing digestive enzymes is produced, usually due to a decreased cell number (Mammalian Phenotype Ontology, MP_0009154)
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3 gene mutations causing the pancreatic acinar hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
PGM3 phosphoglucomutase 3
RHBDF1 rhomboid 5 homolog 1 (Drosophila)
SEC23B Sec23 homolog B (S. cerevisiae)