Congenital Hypoplasia Of Pancreas Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0266267
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Genes

20 genes associated with the disease Congenital Hypoplasia Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
APPL1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1
BLK BLK proto-oncogene, Src family tyrosine kinase
CEL carboxyl ester lipase
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
GATA6 GATA binding protein 6
GCK glucokinase (hexokinase 4)
HNF1A HNF1 homeobox A
HNF1B HNF1 homeobox B
HNF4A hepatocyte nuclear factor 4, alpha
HSP90B1 heat shock protein 90kDa beta (Grp94), member 1
INS insulin
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
KLF11 Kruppel-like factor 11
NEUROD1 neuronal differentiation 1
PAX4 paired box 4
PDX1 pancreatic and duodenal homeobox 1
PTF1A pancreas specific transcription factor, 1a
RFX6 regulatory factor X, 6
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)