abnormal extraembryonic endoderm formation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description malformation of the endoderm of the extraembryonic tissue that appears prior to gastrulation and performs critical functions during embryogenesis including nutrient uptake and transport from the mother to the embryo (Mammalian Phenotype Ontology, MP_0001724)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001724
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Genes

14 gene mutations causing the abnormal extraembryonic endoderm formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FOXD3 forkhead box D3
HAND1 heart and neural crest derivatives expressed 1
HAS2 hyaluronan synthase 2
HNF1B HNF1 homeobox B
HSP90B1 heat shock protein 90kDa beta (Grp94), member 1
HTT huntingtin
LAMTOR1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1
MYL1 myosin, light chain 1, alkali; skeletal, fast
PRICKLE1 prickle homolog 1 (Drosophila)
SMAD2 SMAD family member 2
SNX13 sorting nexin 13
TNRC6A trinucleotide repeat containing 6A
TRIM28 tripartite motif containing 28
WNT3 wingless-type MMTV integration site family, member 3