situs inversus totalis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A left-right reversal (or mirror reflection) of the anatomical location of the major thoracic and abdominal organs. (Human Phenotype Ontology, HP_0001696)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011252
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Genes

17 gene mutations causing the situs inversus totalis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARMC4 armadillo repeat containing 4
BICC1 BicC family RNA binding protein 1
C1ORF127 chromosome 1 open reading frame 127
CCDC151 coiled-coil domain containing 151
CCDC39 coiled-coil domain containing 39
DAW1 dynein assembly factor with WDR repeat domains 1
DCTN5 dynactin 5 (p25)
DNAAF2 dynein, axonemal, assembly factor 2
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
DYX1C1 dyslexia susceptibility 1 candidate 1
FOXJ1 forkhead box J1
NEK8 NIMA-related kinase 8
PSKH1 protein serine kinase H1