fused somites Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	a defect in which there is an appearance of a single enlarged somite resulting from partial or complete fusion of the two somitic anlage (Mammalian Phenotype Ontology, MP_0011733)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011733
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Genes

11 gene mutations causing the fused somites phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
FOXA2	forkhead box A2
FOXH1	forkhead box H1
HES7	hes family bHLH transcription factor 7
LDB1	LIM domain binding 1
MIB1	mindbomb E3 ubiquitin protein ligase 1
NODAL	nodal growth differentiation factor
OTX2	orthodenticle homeobox 2
POFUT1	protein O-fucosyltransferase 1
TBX6	T-box 6
TDGF1	teratocarcinoma-derived growth factor 1
VANGL2	VANGL planar cell polarity protein 2