abnormal cephalic neural fold morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the elevated margins of the neural groove that are located in the future cephalic region of the embryo (Mammalian Phenotype Ontology, MP_0011259)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011259
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9 gene mutations causing the abnormal cephalic neural fold morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AXIN1 axin 1
CNBP CCHC-type zinc finger, nucleic acid binding protein
CSK c-src tyrosine kinase
EFNA5 ephrin-A5
OTX2 orthodenticle homeobox 2
OVOL2 ovo-like zinc finger 2
PDPK1 3-phosphoinositide dependent protein kinase 1
RTEL1 regulator of telomere elongation helicase 1
SSBP3 single stranded DNA binding protein 3