AOPEP aminopeptidase O (putative)
Gene ID: 84909, updated on 17-Aug-2024Gene type: protein coding
Also known as: APO; AP-O; DYT31; ONPEP; C90RF3; C9orf3
- See all available tests in GTR for this gene
- Go to complete Gene record for AOPEP
- Go to Variation Viewer for AOPEP variants
Summary
This gene encodes a member of the M1 zinc aminopeptidase family. The encoded protein is a zinc-dependent metallopeptidase that catalyzes the removal of an amino acid from the amino terminus of a protein or peptide. This protein may play a role in the generation of angiotensin IV. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Dystonia 31 | not available |
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome. GeneReviews: Not available | |
Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. GeneReviews: Not available | |
Meta-analysis identifies six new susceptibility loci for atrial fibrillation. GeneReviews: Not available | |
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. GeneReviews: Not available |
Genomic context
- Location:
- 9q22.32
- Sequence:
- Chromosome: 9; NC_000009.12 (94726699..95150224)
- Total number of exons:
- 32
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for AOPEP variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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