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 (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
13
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Amyotrophic lateral sclerosis Uncertain significance; Conflicting classifications of pathogenicity ClinVar
ClinGen, Disgenet, GenCC, Orphanet
ClinGen, Disgenet, GenCC, Orphanet
ClinGen, Disgenet, GenCC, Orphanet
★★★☆☆
Reported in Unknown/Other Associations (≥2 sources)
AUTISTIC DISORDER CTD, Disgenet
CTD, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis ORPHANET_DG 20368421, 24085347
★★★☆☆
Reported in Unknown/Other Associations (≥2 sources)
Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis GENOMICS_ENGLAND_DG 20368421
★★★☆☆
Reported in Unknown/Other Associations (≥2 sources)
Amyotrophic Lateral Sclerosis Amyotrophic lateral sclerosis Pubtator 23755159, 33051492 Associate
★★★☆☆
Reported in Unknown/Other Associations (≥2 sources)
Amyotrophic lateral sclerosis Amyotrophic Lateral Sclerosis Orphanet
★★★☆☆
Reported in Unknown/Other Associations (≥2 sources)
Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis BEFREE 25604957, 27773581, 28025800, 29194436, 29404340, 29487852, 30206963
★★★☆☆
Reported in Unknown/Other Associations (≥2 sources)
Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis HPO_DG
★★★☆☆
Reported in Unknown/Other Associations (≥2 sources)
Anxiety Anxiety Disorder BEFREE 19729970, 21471957
★☆☆☆☆
Found in Text Mining only
Anxiety Anxiety disorder Pubtator 21471957 Associate
★☆☆☆☆
Found in Text Mining only
Anxiety Anxiety Disorder HPO_DG
★☆☆☆☆
Found in Text Mining only
Anxiety Disorders Anxiety Disorder BEFREE 19729970, 21471957
★☆☆☆☆
Found in Text Mining only