abdominal situs ambiguus Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description an abnormality in which the abdominal organs are positioned in such a way with respect to each other and the left-right axis as to be not clearly lateralised and thus have neither the usual, or normal (situs solitus), nor the mirror-imaged (situs inversus) arrangements (Mammalian Phenotype Ontology, MP_0011250)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011250
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10 gene mutations causing the abdominal situs ambiguus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARMC4 armadillo repeat containing 4
CCDC39 coiled-coil domain containing 39
DAW1 dynein assembly factor with WDR repeat domains 1
DNAAF3 dynein, axonemal, assembly factor 3
DNAH11 dynein, axonemal, heavy chain 11
DNAH5 dynein, axonemal, heavy chain 5
DNAI1 dynein, axonemal, intermediate chain 1
DRC1 dynein regulatory complex subunit 1
IFT27 intraflagellar transport 27
INVS inversin