disorganized embryonic tissue Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a lack of the regular arrangement of any embryonic tissues (Mammalian Phenotype Ontology, MP_0003988)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003988
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Genes

30 gene mutations causing the disorganized embryonic tissue phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR1 activin A receptor, type I
ARC activity-regulated cytoskeleton-associated protein
AXIN1 axin 1
BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase)
BRCA1 breast cancer 1, early onset
BRK1 BRICK1, SCAR/WAVE actin-nucleating complex subunit
CDC42 cell division cycle 42
ESRRB estrogen-related receptor beta
EXT1 exostosin glycosyltransferase 1
FLRT3 fibronectin leucine rich transmembrane protein 3
GINS1 GINS complex subunit 1 (Psf1 homolog)
HNF1B HNF1 homeobox B
HSP90B1 heat shock protein 90kDa beta (Grp94), member 1
HTT huntingtin
MESP1 mesoderm posterior basic helix-loop-helix transcription factor 1
NBN nibrin
NUSAP1 nucleolar and spindle associated protein 1
PAXIP1 PAX interacting (with transcription-activation domain) protein 1
PIK3C3 phosphatidylinositol 3-kinase, catalytic subunit type 3
POFUT2 protein O-fucosyltransferase 2
PPRC1 peroxisome proliferator-activated receptor gamma, coactivator-related 1
PTEN phosphatase and tensin homolog
PTPMT1 protein tyrosine phosphatase, mitochondrial 1
PTPN11 protein tyrosine phosphatase, non-receptor type 11
SMAD1 SMAD family member 1
T T, brachyury homolog (mouse)
TFAP2C transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma)
TJP2 tight junction protein 2
UBA3 ubiquitin-like modifier activating enzyme 3
WNT3 wingless-type MMTV integration site family, member 3