abnormal mesendoderm development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description failure or abnormality in the formation of the embryonic cell layer that gives rise to both the endoderm and mesoderm (Mammalian Phenotype Ontology, MP_0009266)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009266
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11 gene mutations causing the abnormal mesendoderm development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APC adenomatous polyposis coli
COL2A1 collagen, type II, alpha 1
DRAP1 DR1-associated protein 1 (negative cofactor 2 alpha)
FOXH1 forkhead box H1
HIRA histone cell cycle regulator
IFT172 intraflagellar transport 172
NODAL nodal growth differentiation factor
NSD1 nuclear receptor binding SET domain protein 1
OTX2 orthodenticle homeobox 2
SALL4 spalt-like transcription factor 4
TDGF1 teratocarcinoma-derived growth factor 1