right-sided isomerism Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	anomaly in the asymmetry of the visceral paired organs (e.g. lungs) such that organs on the left and right side have the morphology normally seen on the right side of the body; this may also be associated with absence of the spleen (Mammalian Phenotype Ontology, MP_0000508)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000508
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Genes

21 gene mutations causing the right-sided isomerism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
ACVR2B	activin A receptor, type IIB
ANKS6	ankyrin repeat and sterile alpha motif domain containing 6
ATMIN	ATM interactor
C1ORF127	chromosome 1 open reading frame 127
CCDC39	coiled-coil domain containing 39
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
DYX1C1	dyslexia susceptibility 1 candidate 1
FOXJ1	forkhead box J1
GDF1	growth differentiation factor 1
INVS	inversin
MEGF8	multiple EGF-like-domains 8
NEK8	NIMA-related kinase 8
NODAL	nodal growth differentiation factor
PITX2	paired-like homeodomain 2
PKD1L1	polycystic kidney disease 1 like 1
PKD2	polycystic kidney disease 2 (autosomal dominant)
TBC1D32	TBC1 domain family, member 32
ZIC3	Zic family member 3