complete lethality Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description all individuals of a given genotype in a population die before the end of the normal lifespan but time(s) of death are unspecified (Mammalian Phenotype Ontology, MP_0011400)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011400
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Genes

18 gene mutations causing the complete lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASXL1 additional sex combs like transcriptional regulator 1
CLP1 cleavage and polyadenylation factor I subunit 1
FBXW7 F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase
GNAO1 guanine nucleotide binding protein (G protein), alpha activating activity polypeptide O
IKZF1 IKAROS family zinc finger 1 (Ikaros)
INSM1 insulinoma-associated 1
ITGB1 integrin, beta 1 (fibronectin receptor, beta polypeptide, antigen CD29 includes MDF2, MSK12)
MECOM MDS1 and EVI1 complex locus
OCA2 oculocutaneous albinism II
PFN1 profilin 1
PICALM phosphatidylinositol binding clathrin assembly protein
PLK3 polo-like kinase 3
PRPS1 phosphoribosyl pyrophosphate synthetase 1
RUVBL2 RuvB-like AAA ATPase 2
SFPQ splicing factor proline/glutamine-rich
T T, brachyury homolog (mouse)
TCF7L2 transcription factor 7-like 2 (T-cell specific, HMG-box)
VANGL2 VANGL planar cell polarity protein 2