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PIPOX (pipecolic acid and sarcosine oxidase)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51268
Gene nameGene Name - the full gene name approved by the HGNC.
Pipecolic acid and sarcosine oxidase
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
PIPOX
SynonymsGene synonyms aliases
LPIPOX
ChromosomeChromosome number
17
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q11.2
miRNAmiRNA 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 IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
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
Sequence
Sequence length 390
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Glycine, serine and threonine metabolism
Lysine degradation
Metabolic pathways
Peroxisome
  Lysine catabolism
Peroxisomal protein import
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Adrenoleukodystrophy Adrenoleukodystrophy, Neonatal rs128624213, rs128624214, rs1569541109, rs128624215, rs128624216, rs128624217, rs128624218, rs128624219, rs128624220, rs128624221, rs387906494, rs128624222, rs128624223, rs387906495, rs128624224, rs1569541096, rs2147483647, rs128624225, rs11146842, rs4010613, rs387906496, rs1569541198, rs1569540743, rs387906497, rs193922093, rs193922097, rs193922098, rs398123100, rs398123102, rs398123105, rs398123106, rs398123107, rs398123108, rs398123110, rs398123111, rs398123112, rs713993050, rs201568579, rs150346282, rs797044610, rs797044625, rs797044726, rs864309520, rs886044777, rs1057516052, rs1057517954, rs1064793877, rs1131691916, rs1131691743, rs1557054318, rs1557054153, rs1557052302, rs1557052362, rs1557054873, rs1557055340, rs1557052530, rs1557055392, rs1557052171, rs1557054875, rs1557052294, rs1557052390, rs1557052397, rs1557054210, rs1170974058, rs727503786, rs1557055405, rs1557055311, rs1557052555, rs1557052133, rs1159943880, rs1557054776, rs1557052351, rs1557055253, rs1557055398, rs1557052573, rs1557055260, rs1292006620, rs1569540693, rs782266592, rs1557055316, rs1569540676, rs1569541115, rs1569541000, rs1569541088, rs1569541203, rs1569540688, rs1569540883, rs1569541009, rs1569540665, rs1569540695, rs1569540704, rs1569541006, rs781862879, rs1557055337, rs1569541207, rs1603235321, rs1603231653, rs1603231784, rs1603231897, rs1603232111, rs1603232195, rs1603232243, rs1603233089, rs1603233113, rs1603234451, rs1603234759, rs1603235901, rs1603236012, rs1603235263, rs1603235389, rs1603231911, rs1603233120, rs1603234501, rs1603236020, rs1603231848, rs1603232237, rs1603234466, rs1603235267, rs1603235421, rs1603235941, rs1603234574, rs1603236013, rs2091702389, rs2091711094, rs2091711370, rs782509393, rs2091726671, rs2091726809, rs1557054173, rs2091749146, rs2091762383, rs2091763089, rs2091764526, rs2091764754, rs2091774046, rs2091775068, rs2091727061, rs2091708827, rs2091774163, rs2091726242 10642506
Schizophrenia Schizophrenia, Childhood rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 26508570
Unknown
Disease name Disease term dbSNP ID References
Hyperpipecolic acidemia Hyperpipecolic Acidemia 10642506
Mental depression Major Depressive Disorder rs587778876, rs587778877 30718901
Peroxisomal dysfunction Peroxisomal Dysfunction, General, Peroxisomal Dysfunction, Multiple, Peroxisomal Dysfunction, Single 10642506

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