mesocardia Gene Set

Dataset	MPO Gene-Phenotype 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://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000650
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Genes

12 gene mutations causing the mesocardia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
ACVR2B	activin A receptor, type IIB
ARMC4	armadillo repeat containing 4
CFC1	cripto, FRL-1, cryptic family 1
CITED2	Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
DNAH11	dynein, axonemal, heavy chain 11
DNAH5	dynein, axonemal, heavy chain 5
MEGF8	multiple EGF-like-domains 8
MGRN1	mahogunin ring finger 1, E3 ubiquitin protein ligase
PCSK5	proprotein convertase subtilisin/kexin type 5
PKD2	polycystic kidney disease 2 (autosomal dominant)
RFX3	regulatory factor X, 3 (influences HLA class II expression)
TBC1D32	TBC1 domain family, member 32