abnormal extraembryonic ectoderm morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the layer of the ectoderm of the extraembryonic tissue (Mammalian Phenotype Ontology, MP_0010736)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010736
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Genes

20 gene mutations causing the abnormal extraembryonic ectoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR1B activin A receptor, type IB
ARC activity-regulated cytoskeleton-associated protein
ATAD3A ATPase family, AAA domain containing 3A
BMP5 bone morphogenetic protein 5
CUL3 cullin 3
DAG1 dystroglycan 1 (dystrophin-associated glycoprotein 1)
ELF5 E74-like factor 5 (ets domain transcription factor)
MAPK1 mitogen-activated protein kinase 1
NANOG Nanog homeobox
NBN nibrin
NF2 neurofibromin 2 (merlin)
NODAL nodal growth differentiation factor
POFUT2 protein O-fucosyltransferase 2
POU2F1 POU class 2 homeobox 1
PPP1R8 protein phosphatase 1, regulatory subunit 8
SMAD1 SMAD family member 1
SMAD2 SMAD family member 2
TFAP2C transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma)
TRIM33 tripartite motif containing 33
XIST X inactive specific transcript (non-protein coding)