abnormal digestive organ placement Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description different location or arrangement of any of the alimentary tract organs (Mammalian Phenotype Ontology, MP_0003283)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003283
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Genes

27 gene mutations causing the abnormal digestive organ placement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARMC4 armadillo repeat containing 4
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
DAW1 dynein assembly factor with WDR repeat domains 1
DNAAF2 dynein, axonemal, assembly factor 2
DNAH11 dynein, axonemal, heavy chain 11
DNAH5 dynein, axonemal, heavy chain 5
DYX1C1 dyslexia susceptibility 1 candidate 1
FOXJ1 forkhead box J1
IFT122 intraflagellar transport 122
IHH indian hedgehog
INVS inversin
LEFTY2 left-right determination factor 2
MBD4 methyl-CpG binding domain protein 4
MEGF8 multiple EGF-like-domains 8
NKX3-2 NK3 homeobox 2
NODAL nodal growth differentiation factor
PDX1 pancreatic and duodenal homeobox 1
PITX2 paired-like homeodomain 2
PKD1L1 polycystic kidney disease 1 like 1
PKD2 polycystic kidney disease 2 (autosomal dominant)
SHH sonic hedgehog
TBC1D32 TBC1 domain family, member 32
TCTN2 tectonic family member 2
TMEM67 transmembrane protein 67
ZIC3 Zic family member 3