Gene Gene information from NCBI Gene database.
Entrez ID 51268
Gene name Pipecolic acid and sarcosine oxidase
Gene symbol PIPOX
Synonyms (NCBI Gene)
LPIPOX
Chromosome 17
Chromosome location 17q11.2
miRNA miRNA information provided by mirtarbase database.
124
miRTarBase ID miRNA Experiments Reference
MIRT003818 hsa-miR-197-3p Microarray 16822819
MIRT1236069 hsa-miR-1244 CLIP-seq
MIRT1236070 hsa-miR-1257 CLIP-seq
MIRT1236071 hsa-miR-125a-3p CLIP-seq
MIRT1236072 hsa-miR-1275 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21044950
GO:0005777 Component Peroxisome IBA
GO:0005777 Component Peroxisome IDA 10642506
GO:0005777 Component Peroxisome IEA
GO:0005782 Component Peroxisomal matrix TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616713 17804 ENSG00000179761
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9P0Z9
Protein name Peroxisomal sarcosine oxidase (PSO) (EC 1.5.3.1) (EC 1.5.3.7) (L-pipecolate oxidase) (L-pipecolic acid oxidase)
Protein function Metabolizes sarcosine and L-pipecolic acid.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01266 DAO 9 364 FAD dependent oxidoreductase Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in the liver and kidney. {ECO:0000269|PubMed:10642506}.
Sequence
Sequence length 390
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Glycine, serine and threonine metabolism
Lysine degradation
Metabolic pathways
Peroxisome
  Lysine catabolism
Peroxisomal protein import
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
2
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Low-frequency hearing loss Uncertain significance rs747657795 RCV002246212
Low-frequency sensorineural hearing impairment Uncertain significance rs747657795 RCV002246212
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 24884785, 25550822, 26339363
Carcinoma Lobular Associate 25837163
Colorectal Neoplasms Associate 28058013, 34965262
Diabetic Nephropathies Associate 34215202
Neoplasm Metastasis Associate 25550822
Prostatitis Associate 30628163