abnormal large intestine crypts of lieberkuhn morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the tubular intestinal glands found in the mucosal membranes of the large intestine (Mammalian Phenotype Ontology, MP_0004842)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004842
Similar Terms
Downloads & Tools


27 gene mutations causing the abnormal large intestine crypts of lieberkuhn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGR2 anterior gradient 2
APC adenomatous polyposis coli
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
ESR2 estrogen receptor 2 (ER beta)
FGF10 fibroblast growth factor 10
FPR2 formyl peptide receptor 2
GNAI2 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 2
GUCA2A guanylate cyclase activator 2A (guanylin)
HDAC2 histone deacetylase 2
IGF2BP1 insulin-like growth factor 2 mRNA binding protein 1
IL17RE interleukin 17 receptor E
IL22 interleukin 22
KLF5 Kruppel-like factor 5 (intestinal)
KRAS Kirsten rat sarcoma viral oncogene homolog
LTBP4 latent transforming growth factor beta binding protein 4
MUC2 mucin 2, oligomeric mucus/gel-forming
MYC v-myc avian myelocytomatosis viral oncogene homolog
NLRP6 NLR family, pyrin domain containing 6
PRKDC protein kinase, DNA-activated, catalytic polypeptide
PYCARD PYD and CARD domain containing
SAV1 salvador family WW domain containing protein 1
SLC26A3 solute carrier family 26 (anion exchanger), member 3
TLR2 toll-like receptor 2
TMPO thymopoietin
TSTA3 tissue specific transplantation antigen P35B
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor