abnormal penile erection Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description altered ability to achieve a rigid state of the penis obtained in the condition in which the erectile tissue is filled with blood (Mammalian Phenotype Ontology, MP_0001379)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001379
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12 gene mutations causing the abnormal penile erection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADA adenosine deaminase
ADORA2B adenosine A2b receptor
ARNTL aryl hydrocarbon receptor nuclear translocator-like
ATP7A ATPase, Cu++ transporting, alpha polypeptide
HMGA2 high mobility group AT-hook 2
IMMP2L IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae)
NOS3 nitric oxide synthase 3 (endothelial cell)
OTC ornithine carbamoyltransferase
PRKG1 protein kinase, cGMP-dependent, type I
SERPINC1 serpin peptidase inhibitor, clade C (antithrombin), member 1
STAM signal transducing adaptor molecule (SH3 domain and ITAM motif) 1
USP14 ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase)