abnormal paneth cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the large secretory cells containing coarse granules found at the base of the crypts of Lieberkuhn in the small intestine (Mammalian Phenotype Ontology, MP_0004843)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004843
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Genes

12 gene mutations causing the abnormal paneth cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGR2 anterior gradient 2
ATG16L1 autophagy related 16-like 1 (S. cerevisiae)
CBFA2T2 core-binding factor, runt domain, alpha subunit 2; translocated to, 2
FEN1 flap structure-specific endonuclease 1
FOXL1 forkhead box L1
HPRT1 hypoxanthine phosphoribosyltransferase 1
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
MYC v-myc avian myelocytomatosis viral oncogene homolog
NRIP1 nuclear receptor interacting protein 1
SEC23B Sec23 homolog B (S. cerevisiae)
SPDEF SAM pointed domain containing ETS transcription factor
YIPF6 Yip1 domain family, member 6