Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51268
Gene name Gene Name - the full gene name approved by the HGNC.
Pipecolic acid and sarcosine oxidase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PIPOX
Synonyms (NCBI Gene) Gene synonyms aliases
LPIPOX
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q11.2
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21044950
GO:0005777 Component Peroxisome IBA 21873635
GO:0005777 Component Peroxisome IDA 10642506
GO:0005782 Component Peroxisomal matrix TAS
GO:0005829 Component Cytosol TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616713 17804 ENSG00000179761
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Adrenoleukodystrophy Adrenoleukodystrophy, Neonatal rs128624213, rs128624214, rs1569541109, rs128624215, rs128624216, rs128624217, rs128624218, rs128624219, rs128624220, rs128624221, rs387906494, rs128624222, rs128624223, rs387906495, rs128624224
View all (125 more)
10642506
Schizophrenia Schizophrenia, Childhood rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
26508570
Unknown
Disease term Disease name Evidence References Source
Mental depression Major Depressive Disorder 30718901 ClinVar
Gout Gout GWAS
Mental Depression Mental Depression GWAS
Oligodendroglioma Oligodendroglioma GWAS
Associations from Text Mining
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