Gene Gene information from NCBI Gene database.
Entrez ID 1610
Gene name D-amino acid oxidase
Gene symbol DAO
Synonyms (NCBI Gene)
DAAODAMOXOXDA
Chromosome 12
Chromosome location 12q24.11
Summary This gene encodes the peroxisomal enzyme D-amino acid oxidase. The enzyme is a flavoprotein which uses flavin adenine dinucleotide (FAD) as its prosthetic group. Its substrates include a wide variety of D-amino acids, but it is inactive on the naturally o
miRNA miRNA information provided by mirtarbase database.
47
miRTarBase ID miRNA Experiments Reference
MIRT724913 hsa-miR-4269 HITS-CLIP 19536157
MIRT724912 hsa-miR-6715b-5p HITS-CLIP 19536157
MIRT724911 hsa-miR-4645-5p HITS-CLIP 19536157
MIRT724910 hsa-miR-4673 HITS-CLIP 19536157
MIRT724909 hsa-miR-5088-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
50
GO ID Ontology Definition Evidence Reference
GO:0003884 Function D-amino-acid oxidase activity IBA
GO:0003884 Function D-amino-acid oxidase activity IDA 12364586, 16616139, 17303072, 18544534, 19309736, 20567862, 20603179, 23219954, 29274788, 29326945, 32730563
GO:0003884 Function D-amino-acid oxidase activity IEA
GO:0003884 Function D-amino-acid oxidase activity IMP 29274788
GO:0005515 Function Protein binding IPI 12364586, 20521334, 21679769, 21988832, 24722188, 25416956, 28514442, 29274788, 31515488, 33961781
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
124050 2671 ENSG00000110887
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P14920
Protein name D-amino-acid oxidase (DAAO) (DAMOX) (DAO) (EC 1.4.3.3)
Protein function Catalyzes the oxidative deamination of D-amino acids with broad substrate specificity (PubMed:16616139, PubMed:17088322, PubMed:17303072, PubMed:18544534, PubMed:20368421, PubMed:20567862, PubMed:20603179, PubMed:22203986, PubMed:23219954, PubMe
PDB 2DU8 , 2E48 , 2E49 , 2E4A , 2E82 , 3CUK , 3G3E , 3W4I , 3W4J , 3W4K , 3ZNN , 3ZNO , 3ZNP , 3ZNQ , 4QFC , 4QFD , 5ZJ9 , 5ZJA , 6KBP , 7U9S , 7U9U , 8HY5
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01266 DAO 2 329 FAD dependent oxidoreductase Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in the cerebellum, in astrocytes of the cortex, in motor neurons and fibers of the lumbar spinal cord (at protein level) (PubMed:17880399, PubMed:18544534, PubMed:18560437, PubMed:24138986, PubMed:34041270). Expressed in gobl
Sequence
Sequence length 347
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Glycine, serine and threonine metabolism
Arginine and proline metabolism
D-Amino acid metabolism
Metabolic pathways
Peroxisome
  Glyoxylate metabolism and glycine degradation
Peroxisomal protein import
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
39
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Amyotrophic lateral sclerosis Uncertain significance; Conflicting classifications of pathogenicity rs373913310, rs778735604, rs138277420, rs2039610204, rs781658657 RCV001843917
RCV001095492
RCV001095493
RCV001095495
RCV001260559
Cholangiocarcinoma Benign rs7980427 RCV005920343
DAO-related disorder Benign; Uncertain significance; Likely benign; Conflicting classifications of pathogenicity rs7980427, rs531892910, rs773765064, rs368093324, rs2039476497, rs760432003, rs372560295, rs147144733, rs143732132, rs139166976, rs200350184, rs146917361, rs181080261, rs779881826, rs768403852
View all (17 more)
RCV003975995
RCV003402634
RCV003414528
RCV003414555
RCV003400183
RCV003419090
RCV003392849
RCV003418824
RCV003946633
RCV003919573
RCV003964569
RCV003912267
RCV003899298
RCV003911670
RCV003914028
RCV003951953
RCV003949450
RCV003969337
RCV003949160
RCV003946805
RCV003946946
RCV003956731
RCV003969689
RCV003954796
RCV003969081
RCV003910811
RCV003968184
RCV003912842
RCV003932958
RCV003933002
RCV003396745
RCV003399030
Thymoma Benign rs7980427 RCV005920342
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Amyotrophic Lateral Sclerosis Associate 23755159, 33051492
Anxiety Associate 21471957
Bipolar Disorder Associate 16380905
Carcinoma Renal Cell Associate 38297313
Colorectal Neoplasms Associate 33540681
Darier Disease Associate 26440917
Drug Related Side Effects and Adverse Reactions Stimulate 33540681
Exostoses Associate 34582124
Glioblastoma Associate 33540681
Glutamate formiminotransferase deficiency Associate 19077230