delayed intestine development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description slowed progression to a structurally mature intestine (Mammalian Phenotype Ontology, MP_0000478)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000478
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Genes

5 gene mutations causing the delayed intestine development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ERCC5 excision repair cross-complementation group 5
FOXL1 forkhead box L1
IGF2BP1 insulin-like growth factor 2 mRNA binding protein 1
NKX2-3 NK2 homeobox 3
PEX5 peroxisomal biogenesis factor 5