abnormal cranial flexure morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly or absence of the sharp, ventrally concave bend in the developing midbrain of the embryo (Mammalian Phenotype Ontology, MP_0004203)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004203
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7 gene mutations causing the abnormal cranial flexure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
C2CD3 C2 calcium-dependent domain containing 3
ERBB3 erb-b2 receptor tyrosine kinase 3
IFT57 intraflagellar transport 57
IFT88 intraflagellar transport 88
INTU inturned planar cell polarity protein
REST RE1-silencing transcription factor
WNT1 wingless-type MMTV integration site family, member 1