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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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