partial embryonic lethality between implantation and somite formation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between the point of implantation and somite formation (Mus: E4.5 to less than E8) (Mammalian Phenotype Ontology, MP_0011106)
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21 gene mutations causing the partial embryonic lethality between implantation and somite formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AMOT angiomotin
APC adenomatous polyposis coli
CDK2AP1 cyclin-dependent kinase 2 associated protein 1
DAD1 defender against cell death 1
DSG2 desmoglein 2
EGFR epidermal growth factor receptor
FGFR1 fibroblast growth factor receptor 1
GAPDH glyceraldehyde-3-phosphate dehydrogenase
GDF3 growth differentiation factor 3
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
LIG3 ligase III, DNA, ATP-dependent
NELFB negative elongation factor complex member B
NF2 neurofibromin 2 (merlin)
NFE2L1 nuclear factor, erythroid 2-like 1
NR5A2 nuclear receptor subfamily 5, group A, member 2
RAI1 retinoic acid induced 1
RANGAP1 Ran GTPase activating protein 1
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
SMAD4 SMAD family member 4
TFAP2C transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma)
WDR1 WD repeat domain 1