abnormal neural plate morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the flat, thickened layer of ectodermal cells in the neuroectodermal area of the embryo's dorsal surface that develops into the neural tube and neural crest (Mammalian Phenotype Ontology, MP_0005657)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005657
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24 gene mutations causing the abnormal neural plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AXIN2 axin 2
CFL1 cofilin 1 (non-muscle)
CHMP5 charged multivesicular body protein 5
CHRD chordin
DISP1 dispatched homolog 1 (Drosophila)
EPB41L5 erythrocyte membrane protein band 4.1 like 5
FGFR1 fibroblast growth factor receptor 1
FOXH1 forkhead box H1
FURIN furin (paired basic amino acid cleaving enzyme)
GNB1 guanine nucleotide binding protein (G protein), beta polypeptide 1
HIRA histone cell cycle regulator
JARID2 jumonji, AT rich interactive domain 2
LDB1 LIM domain binding 1
NOG noggin
PNPLA6 patatin-like phospholipase domain containing 6
POGLUT1 protein O-glucosyltransferase 1
QKI QKI, KH domain containing, RNA binding
SMO smoothened, frizzled class receptor
SSBP3 single stranded DNA binding protein 3
TCOF1 Treacher Collins-Franceschetti syndrome 1
VANGL2 VANGL planar cell polarity protein 2
ZEB2 zinc finger E-box binding homeobox 2
ZIC2 Zic family member 2
ZIC3 Zic family member 3