mesocardia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Mesocardia is a abnormal location of the heart in which the heart is in a midline position and the longitudinal axis of the heart lies in the mid-sagittal plane. (Human Phenotype Ontology, HP_0011599)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011599
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Genes

2 genes associated with the mesocardia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CFC1 cripto, FRL-1, cryptic family 1
SRCAP Snf2-related CREBBP activator protein