absent paraxial mesoderm Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence or loss of the mesoderm normally found at either side of the midline embryonic notochord that, on segmentation, forms the paired somites. (Mammalian Phenotype Ontology, MP_0012184)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012184
Similar Terms
Downloads & Tools

Genes

7 gene mutations causing the absent paraxial mesoderm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DDX11 DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11
DRAP1 DR1-associated protein 1 (negative cofactor 2 alpha)
LRP6 low density lipoprotein receptor-related protein 6
MECOM MDS1 and EVI1 complex locus
MESP1 mesoderm posterior basic helix-loop-helix transcription factor 1
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
MSGN1 mesogenin 1