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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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