abnormal embryonic neuroepithelial cell proliferation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the ability of the cells of the embryonic neuroepithelium to undergo expansion by cell division (Mammalian Phenotype Ontology, MP_0012704)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012704
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10 gene mutations causing the abnormal embryonic neuroepithelial cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AMBRA1 autophagy/beclin-1 regulator 1
CNBP CCHC-type zinc finger, nucleic acid binding protein
LEP leptin
LMO4 LIM domain only 4
NODAL nodal growth differentiation factor
OVOL2 ovo-like zinc finger 2
RAD54L2 RAD54-like 2 (S. cerevisiae)
SCUBE1 signal peptide, CUB domain, EGF-like 1
TCOF1 Treacher Collins-Franceschetti syndrome 1
TP53BP2 tumor protein p53 binding protein 2