common atrium Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Complete absence of the interatrial septum with common atrioventricular valve and two atrioventricular connections. (Human Phenotype Ontology, HP_0011565)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010406
Similar Terms
Downloads & Tools

Genes

14 gene mutations causing the common atrium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
C5ORF42 chromosome 5 open reading frame 42
CC2D2A coiled-coil and C2 domain containing 2A
CFC1 cripto, FRL-1, cryptic family 1
CITED2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
DNAH5 dynein, axonemal, heavy chain 5
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
IFT74 intraflagellar transport 74
IFT88 intraflagellar transport 88
LTBP1 latent transforming growth factor beta binding protein 1
NODAL nodal growth differentiation factor
OSR1 odd-skipped related transciption factor 1
PCSK6 proprotein convertase subtilisin/kexin type 6
PITX2 paired-like homeodomain 2
TBX5 T-box 5