failure to form blastocele Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description developmental anomaly resulting in the absence of the cavity in the blastocyst of the developing embryo (Mammalian Phenotype Ontology, MP_0002663)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002663
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Genes

23 gene mutations causing the failure to form blastocele phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AATF apoptosis antagonizing transcription factor
BIRC5 baculoviral IAP repeat containing 5
CDH1 cadherin 1, type 1, E-cadherin (epithelial)
CTNNA1 catenin (cadherin-associated protein), alpha 1, 102kDa
EMG1 EMG1 N1-specific pseudouridine methyltransferase
FBXO5 F-box protein 5
FGFR2 fibroblast growth factor receptor 2
GNL3 guanine nucleotide binding protein-like 3 (nucleolar)
HNF1B HNF1 homeobox B
INCENP inner centromere protein antigens 135/155kDa
ITGB1 integrin, beta 1 (fibronectin receptor, beta polypeptide, antigen CD29 includes MDF2, MSK12)
KLF5 Kruppel-like factor 5 (intestinal)
LAMA1 laminin, alpha 1
NOC3L nucleolar complex associated 3 homolog (S. cerevisiae)
PCYT1A phosphate cytidylyltransferase 1, choline, alpha
PIKFYVE phosphoinositide kinase, FYVE finger containing
PLCB3 phospholipase C, beta 3 (phosphatidylinositol-specific)
POLR1B polymerase (RNA) I polypeptide B, 128kDa
RPL38 ribosomal protein L38
SERPINB5 serpin peptidase inhibitor, clade B (ovalbumin), member 5
SMN1 survival of motor neuron 1, telomeric
TEAD4 TEA domain family member 4
WDR36 WD repeat domain 36