neural tube degeneration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a retrogressive impairment of function or destruction of the hollow epithelial tube found on the dorsal side of the vertebrate embryo that develops into the central nervous system (i.e. brain and spinal cord) (Mammalian Phenotype Ontology, MP_0012509)
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4 gene mutations causing the neural tube degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DPH3 diphthamide biosynthesis 3
KIF3A kinesin family member 3A
PTPN12 protein tyrosine phosphatase, non-receptor type 12
REV3L REV3-like, polymerase (DNA directed), zeta, catalytic subunit