abnormal pancreatic acinar cell zymogen granule morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of a membrane-bounded, cytoplasmic secretory granule found in pancreatic acinar cells and contains inactive digestive enzyme precursors (Mammalian Phenotype Ontology, MP_0009160)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009160
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Genes

16 gene mutations causing the abnormal pancreatic acinar cell zymogen granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AQP12A aquaporin 12A
ATF4 activating transcription factor 4
BHLHA15 basic helix-loop-helix family, member a15
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
NEUROD1 neuronal differentiation 1
NEUROG3 neurogenin 3
PPT2 palmitoyl-protein thioesterase 2
RHBDF1 rhomboid 5 homolog 1 (Drosophila)
RPH3AL rabphilin 3A-like (without C2 domains)
SC5D sterol-C5-desaturase
SEC23B Sec23 homolog B (S. cerevisiae)
SERPINI2 serpin peptidase inhibitor, clade I (pancpin), member 2
SYTL1 synaptotagmin-like 1
TK1 thymidine kinase 1, soluble
VAMP8 vesicle-associated membrane protein 8