Gene Gene information from NCBI Gene database.
Entrez ID 26002
Gene name Monooxygenase DBH like 1
Gene symbol MOXD1
Synonyms (NCBI Gene)
MOXPRO5780dJ248E1.1
Chromosome 6
Chromosome location 6q23.2
miRNA miRNA information provided by mirtarbase database.
218
miRTarBase ID miRNA Experiments Reference
MIRT030822 hsa-miR-21-5p Microarray 18591254
MIRT048720 hsa-miR-96-5p CLASH 23622248
MIRT053409 hsa-miR-591 Microarray 23807165
MIRT1155888 hsa-let-7a CLIP-seq
MIRT1155889 hsa-let-7b CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0003824 Function Catalytic activity IEA
GO:0004497 Function Monooxygenase activity IEA
GO:0004500 Function Dopamine beta-monooxygenase activity IBA
GO:0004500 Function Dopamine beta-monooxygenase activity IEA
GO:0005507 Function Copper ion binding IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609000 21063 ENSG00000079931
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6UVY6
Protein name DBH-like monooxygenase protein 1 (EC 1.14.17.-) (Monooxygenase X)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03351 DOMON 33 148 DOMON domain Domain
PF01082 Cu2_monooxygen 187 315 Copper type II ascorbate-dependent monooxygenase, N-terminal domain Domain
PF03712 Cu2_monoox_C 334 491 Copper type II ascorbate-dependent monooxygenase, C-terminal domain Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in lung, kidney, brain and spinal cord. {ECO:0000269|PubMed:15337741, ECO:0000269|PubMed:9751809}.
Sequence
Sequence length 613
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
BREAST CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OBESITY GWAS catalog
★★☆☆☆
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
Asthma Asthma BEFREE 30986547
★☆☆☆☆
Found in Text Mining only
Excessive tearing Excessive Tearing BEFREE 31751751
★☆☆☆☆
Found in Text Mining only
Idiopathic Pulmonary Fibrosis Idiopathic pulmonary fibrosis Pubtator 37085855 Associate
★☆☆☆☆
Found in Text Mining only
Osteomyelitis Osteomyelitis BEFREE 30892092
★☆☆☆☆
Found in Text Mining only
Schizophrenia Schizophrenia BEFREE 15329799
★☆☆☆☆
Found in Text Mining only
Schizophrenia Schizophrenia Pubtator 15329799 Associate
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Stomach neoplasms Pubtator 38200441 Associate
★☆☆☆☆
Found in Text Mining only