decreased embryonic neuroepithelium thickness Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced 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_0012703)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012703
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Genes

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

Symbol Name
CFL1 cofilin 1 (non-muscle)
CHD7 chromodomain helicase DNA binding protein 7
CSK c-src tyrosine kinase
CTBP2 C-terminal binding protein 2
DNM1L dynamin 1-like
FOLR1 folate receptor 1 (adult)
G6PD glucose-6-phosphate dehydrogenase
HESX1 HESX homeobox 1
ISL1 ISL LIM homeobox 1
LEP leptin
OTX2 orthodenticle homeobox 2
PAK4 p21 protein (Cdc42/Rac)-activated kinase 4
TCEB3 transcription elongation factor B (SIII), polypeptide 3 (110kDa, elongin A)
TULP3 tubby like protein 3
VCL vinculin