Gene Gene information from NCBI Gene database.
Entrez ID 8564
Gene name Kynurenine 3-monooxygenase
Gene symbol KMO
Synonyms (NCBI Gene)
dJ317G22.1
Chromosome 1
Chromosome location 1q43
Summary This gene encodes a mitochondrion outer membrane protein that catalyzes the hydroxylation of L-tryptophan metabolite, L-kynurenine, to form L-3-hydroxykynurenine. Studies in yeast identified this gene as a therapeutic target for Huntington disease. [provi
miRNA miRNA information provided by mirtarbase database.
167
miRTarBase ID miRNA Experiments Reference
MIRT512965 hsa-miR-4803 PAR-CLIP 22012620
MIRT512964 hsa-miR-302f PAR-CLIP 22012620
MIRT528926 hsa-miR-501-3p PAR-CLIP 22012620
MIRT528925 hsa-miR-502-3p PAR-CLIP 22012620
MIRT512962 hsa-miR-3143 PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
41
GO ID Ontology Definition Evidence Reference
GO:0004497 Function Monooxygenase activity IEA
GO:0004502 Function Kynurenine 3-monooxygenase activity IBA
GO:0004502 Function Kynurenine 3-monooxygenase activity IDA 9237672, 10672018, 23575632, 26752518, 29208702, 29429898
GO:0004502 Function Kynurenine 3-monooxygenase activity IEA
GO:0004502 Function Kynurenine 3-monooxygenase activity TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603538 6381 ENSG00000117009
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O15229
Protein name Kynurenine 3-monooxygenase (EC 1.14.13.9) (Kynurenine 3-hydroxylase)
Protein function Catalyzes the hydroxylation of L-kynurenine (L-Kyn) to form 3-hydroxy-L-kynurenine (L-3OHKyn) (PubMed:23575632, PubMed:26752518, PubMed:28604669, PubMed:29208702, PubMed:29429898). Required for synthesis of quinolinic acid, a neurotoxic NMDA rec
PDB 5X68
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01494 FAD_binding_3 8 331 FAD binding domain Family
Tissue specificity TISSUE SPECIFICITY: Highest levels in placenta and liver. Detectable in kidney. {ECO:0000269|PubMed:9237672}.
Sequence
Sequence length 486
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Tryptophan metabolism
Metabolic pathways
Biosynthesis of cofactors
  Tryptophan catabolism
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
4
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Benign rs142152979 RCV005906561
Clear cell carcinoma of kidney Benign rs142152979 RCV005906562
KMO-related disorder Likely benign rs200044625 RCV003911736
Lung cancer Benign rs142152979 RCV005906563
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adjustment Disorders Associate 25540092
Aneurysm Associate 33298635
Bipolar Disorder Associate 23459468
Breast Neoplasms Stimulate 33109232
Breast Neoplasms Associate 33887987
Carcinogenesis Associate 33887987
Carcinoma Hepatocellular Associate 26099564
Carcinoma Non Small Cell Lung Associate 23006423
Carcinoma Renal Cell Associate 32390008
Carcinoma Renal Cell Stimulate 38183155