abnormality of placental membranes Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011409
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Genes

9 genes associated with the abnormality of placental membranes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHRNA1 cholinergic receptor, nicotinic, alpha 1 (muscle)
CHRND cholinergic receptor, nicotinic, delta (muscle)
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
FERMT1 fermitin family member 1
GJB2 gap junction protein, beta 2, 26kDa
GLE1 GLE1 RNA export mediator
NSDHL NAD(P) dependent steroid dehydrogenase-like
POMP proteasome maturation protein
RAPSN receptor-associated protein of the synapse