decreased paraxial mesoderm size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size or deficiency of the mesoderm lying at either side of the midline embryonic notochord that, on segmentation, forms the paired somites (Mammalian Phenotype Ontology, MP_0012183)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012183
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Genes

8 gene mutations causing the decreased paraxial mesoderm size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DDX11 DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11
EPB41L5 erythrocyte membrane protein band 4.1 like 5
EXOC4 exocyst complex component 4
FGFR1 fibroblast growth factor receptor 1
ITGA5 integrin, alpha 5 (fibronectin receptor, alpha polypeptide)
MIXL1 Mix paired-like homeobox
NUP133 nucleoporin 133kDa
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha