abdominal situs inversus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A left-right reversal (or mirror reflection) of the anatomical location of the viscera of the abdomen. (Human Phenotype Ontology, HP_0003363)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003363
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Genes

10 genes associated with the abdominal situs inversus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTG2 actin, gamma 2, smooth muscle, enteric
CFAP53 cilia and flagella associated protein 53
CFC1 cripto, FRL-1, cryptic family 1
LETM1 leucine zipper-EF-hand containing transmembrane protein 1
NELFA negative elongation factor complex member A
NODAL nodal growth differentiation factor
OTX2 orthodenticle homeobox 2
PRRX1 paired related homeobox 1
WHSC1 Wolf-Hirschhorn syndrome candidate 1
ZIC3 Zic family member 3