increased embryonic neuroepithelium thickness Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased width of the epithelial cell layer that lines the neural tube and develops into the nervous system and into the neural crest cells (Mammalian Phenotype Ontology, MP_0012702)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012702
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Genes

7 gene mutations causing the increased embryonic neuroepithelium thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALX1 ALX homeobox 1
APAF1 apoptotic peptidase activating factor 1
BRD2 bromodomain containing 2
HLA-DOA major histocompatibility complex, class II, DO alpha
ITGB1 integrin, beta 1 (fibronectin receptor, beta polypeptide, antigen CD29 includes MDF2, MSK12)
OVOL2 ovo-like zinc finger 2
SCUBE1 signal peptide, CUB domain, EGF-like 1