complete embryonic lethality at implantation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description death of all organisms of a given genotype in a population at the point of implantation (Mus: E4.5) (Mammalian Phenotype Ontology, MP_0011093)
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21 gene mutations causing the complete embryonic lethality at implantation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACTB actin, beta
ASIP agouti signaling protein
B3GALNT1 beta-1,3-N-acetylgalactosaminyltransferase 1 (globoside blood group)
CNOT3 CCR4-NOT transcription complex, subunit 3
DSG2 desmoglein 2
EGFR epidermal growth factor receptor
FLII flightless I homolog (Drosophila)
HSPA5 heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa)
KLF5 Kruppel-like factor 5 (intestinal)
MBTPS1 membrane-bound transcription factor peptidase, site 1
MCL1 myeloid cell leukemia 1
NUSAP1 nucleolar and spindle associated protein 1
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
PKM pyruvate kinase, muscle
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
TBP TATA box binding protein
THOC1 THO complex 1
TOPBP1 topoisomerase (DNA) II binding protein 1
TYR tyrosinase
VEZT vezatin, adherens junctions transmembrane protein
ZNF830 zinc finger protein 830