absent heart Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	absence of the hollow, muscular organ that maintains the circulation of the blood (Mammalian Phenotype Ontology, MP_0011388)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011388
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Genes

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

Symbol	Name
FGF8	fibroblast growth factor 8 (androgen-induced)
LDB1	LIM domain binding 1
LEFTY2	left-right determination factor 2
MESP1	mesoderm posterior basic helix-loop-helix transcription factor 1
MESP2	mesoderm posterior basic helix-loop-helix transcription factor 2
MLLT4	myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 4
MTERF4	mitochondrial transcription termination factor 4
OTX2	orthodenticle homeobox 2
PDPK1	3-phosphoinositide dependent protein kinase 1
TCF7L1	transcription factor 7-like 1 (T-cell specific, HMG-box)
TFB1M	transcription factor B1, mitochondrial