abnormal neural fold elevation formation Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	any anomaly in the process by which the lateral borders of the neural plate begin to migrate upwards to form the neural folds, caused by the proliferation of the underlying mesoderm (Mammalian Phenotype Ontology, MP_0004838)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004838
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Genes

10 gene mutations causing the abnormal neural fold elevation formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
BCL10	B-cell CLL/lymphoma 10
CSNK2A1	casein kinase 2, alpha 1 polypeptide
GRHL2	grainyhead-like 2 (Drosophila)
HECTD1	HECT domain containing E3 ubiquitin protein ligase 1
LMO4	LIM domain only 4
MIXL1	Mix paired-like homeobox
PAX3	paired box 3
POR	P450 (cytochrome) oxidoreductase
SMARCC1	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1
TFAP2A	transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)