absent midbrain-hindbrain boundary Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the midbrain-hindbrain domain of the embryonic brain that is comprised of the mesencephalic vesicle and the first rhombencephalic vesicle at early somitogenesis stages; normally, an organizing center located at the boundary patterns the midbrain and hindbrain primordia of the neural plate (Mammalian Phenotype Ontology, MP_0012133)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012133
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Genes

4 gene mutations causing the absent midbrain-hindbrain boundary phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
LDB1 LIM domain binding 1
LMX1B LIM homeobox transcription factor 1, beta
PAX2 paired box 2
WNT1 wingless-type MMTV integration site family, member 1