Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1610
Gene name Gene Name - the full gene name approved by the HGNC.
D-amino acid oxidase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DAO
Synonyms (NCBI Gene) Gene synonyms aliases
DAAO, DAMOX, OXDA
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q24.11
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003884 Function D-amino-acid oxidase activity IBA 21873635
GO:0003884 Function D-amino-acid oxidase activity IDA 12364586, 16616139, 17303072, 18544534, 19309736, 20603179
GO:0005515 Function Protein binding IPI 12364586, 20521334, 21679769, 21988832, 24722188, 25416956, 31515488
GO:0005737 Component Cytoplasm IBA 21873635
GO:0005741 Component Mitochondrial outer membrane IDA 21679769
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
124050 2671 ENSG00000110887
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Amyotrophic lateral sclerosis Amyotrophic Lateral Sclerosis, Amyotrophic lateral sclerosis rs267607084, rs312262720, rs312262752, rs121908287, rs121908288, rs29001584, rs28941475, rs121434378, rs386134173, rs386134174, rs80356730, rs80356727, rs4884357, rs80356717, rs80356733
View all (171 more)
20368421, 24085347
Autism Autistic Disorder rs121964908, rs62643608, rs181327458, rs797046134, rs869312704, rs1555013332, rs876657679, rs1057518999, rs1057518658, rs771827120, rs1555187899, rs773080572, rs753871454, rs1684130791, rs1684180699
View all (8 more)
17629951
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
18583979
Unknown
Disease term Disease name Evidence References Source
Major affective disorder MAJOR AFFECTIVE DISORDER 2 18165970 ClinVar
Mental depression Depressive disorder ClinVar
Alzheimer disease Alzheimer disease GWAS
Associations from Text Mining
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