cardia bifida Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	failure of the bilateral myocardial cells to coalesce into a single central heart tube resulting in the presence of two independent hearts (Mammalian Phenotype Ontology, MP_0004187)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004187
Similar Terms
Downloads & Tools

Genes

16 gene mutations causing the cardia bifida phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
ALG13	ALG13, UDP-N-acetylglucosaminyltransferase subunit
APC	adenomatous polyposis coli
AXIN1	axin 1
AXIN2	axin 2
CHMP5	charged multivesicular body protein 5
FLRT3	fibronectin leucine rich transmembrane protein 3
FOXP4	forkhead box P4
FURIN	furin (paired basic amino acid cleaving enzyme)
GATA4	GATA binding protein 4
HGS	hepatocyte growth factor-regulated tyrosine kinase substrate
HIF1A	hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
MESP1	mesoderm posterior basic helix-loop-helix transcription factor 1
NCKAP1	NCK-associated protein 1
OVOL2	ovo-like zinc finger 2
POGLUT1	protein O-glucosyltransferase 1
PTEN	phosphatase and tensin homolog