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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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)