abnormality of abdominal situs Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the abdominal situs, i.e., of the sidedness of the abdomin and its organs. (Human Phenotype Ontology, HP_0011620)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011620
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10 genes associated with the abnormality of abdominal situs 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