abnormal pancreas development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the formation of the organ that secretes pancreatic juice into the duodenum and secretes glucagon and insulin into the bloodstream (Mammalian Phenotype Ontology, MP_0003934)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003934
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23 gene mutations causing the abnormal pancreas development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
DLL1 delta-like 1 (Drosophila)
FGFR2 fibroblast growth factor receptor 2
GDF11 growth differentiation factor 11
HES1 hes family bHLH transcription factor 1
HHIP hedgehog interacting protein
ILDR2 immunoglobulin-like domain containing receptor 2
INSM1 insulinoma-associated 1
ISL1 ISL LIM homeobox 1
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
MNX1 motor neuron and pancreas homeobox 1
NKX2-2 NK2 homeobox 2
NKX3-2 NK3 homeobox 2
ONECUT1 one cut homeobox 1
PAX6 paired box 6
PCSK2 proprotein convertase subtilisin/kexin type 2
PDX1 pancreatic and duodenal homeobox 1
PTF1A pancreas specific transcription factor, 1a
SEC23B Sec23 homolog B (S. cerevisiae)
SEL1L sel-1 suppressor of lin-12-like (C. elegans)
SPEN spen family transcriptional repressor
STARD13 StAR-related lipid transfer (START) domain containing 13
TLE3 transducin-like enhancer of split 3