absent inner cell mass Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the cells of the blastocyst that develop into the body of the embryo (Mammalian Phenotype Ontology, MP_0004964)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004964
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Genes

17 gene mutations causing the absent inner cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CSNK2B casein kinase 2, beta polypeptide
CTNNA1 catenin (cadherin-associated protein), alpha 1, 102kDa
DMBT1 deleted in malignant brain tumors 1
EMG1 EMG1 N1-specific pseudouridine methyltransferase
FEN1 flap structure-specific endonuclease 1
GMNN geminin, DNA replication inhibitor
GNL3 guanine nucleotide binding protein-like 3 (nucleolar)
INCENP inner centromere protein antigens 135/155kDa
ITGB1 integrin, beta 1 (fibronectin receptor, beta polypeptide, antigen CD29 includes MDF2, MSK12)
NELFB negative elongation factor complex member B
POLR1B polymerase (RNA) I polypeptide B, 128kDa
POT1 protection of telomeres 1
POU5F1 POU class 5 homeobox 1
RACGAP1 Rac GTPase activating protein 1
TADA3 transcriptional adaptor 3
THOC1 THO complex 1
TRRAP transformation/transcription domain-associated protein