situs ambiguus Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A physical disorder characterized by the abnormal distribution of the major visceral organs within the chest and abdomen. (Human Disease Ontology, DOID_0050545)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002767
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Genes

7 gene mutations causing the situs ambiguus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BICC1 BicC family RNA binding protein 1
DYX1C1 dyslexia susceptibility 1 candidate 1
INVS inversin
NODAL nodal growth differentiation factor
PKD2 polycystic kidney disease 2 (autosomal dominant)
TGIF1 TGFB-induced factor homeobox 1
ZIC3 Zic family member 3