delayed somite formation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description late onset of the induction and/or differentiation of the somites (Mammalian Phenotype Ontology, MP_0003794)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003794
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Genes

11 gene mutations causing the delayed somite formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CYFIP1 cytoplasmic FMR1 interacting protein 1
DLL3 delta-like 3 (Drosophila)
FOXF1 forkhead box F1
ITGB1 integrin, beta 1 (fibronectin receptor, beta polypeptide, antigen CD29 includes MDF2, MSK12)
KDM6A lysine (K)-specific demethylase 6A
LMO2 LIM domain only 2 (rhombotin-like 1)
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
MYF5 myogenic factor 5
NOTCH1 notch 1
TACC3 transforming, acidic coiled-coil containing protein 3
TMED2 transmembrane emp24 domain trafficking protein 2