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Gene Gene information from NCBI Gene database.
Entrez ID 2327
Gene name Flavin containing dimethylaniline monoxygenase 2
Gene symbol FMO2
Synonyms (NCBI Gene)
FMO1B1
Chromosome 1
Chromosome location 1q24.3
Summary This gene encodes a flavin-containing monooxygenase family member. It is an NADPH-dependent enzyme that catalyzes the N-oxidation of some primary alkylamines through an N-hydroxylamine intermediate. However, some human populations contain an allele (FMO2*
miRNA miRNA information provided by mirtarbase database.
233 Show/Hide all (233)
miRTarBase ID miRNA Experiments Reference
MIRT999691 hsa-let-7a CLIP-seq
MIRT999692 hsa-let-7b CLIP-seq
MIRT999693 hsa-let-7c CLIP-seq
MIRT999694 hsa-let-7d CLIP-seq
MIRT999695 hsa-let-7e CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
21 Show/Hide all (21)
GO ID Ontology Definition Evidence Reference
GO:0004497 Function Monooxygenase activity IEA
GO:0004499 Function N,N-dimethylaniline monooxygenase activity IBA
GO:0004499 Function N,N-dimethylaniline monooxygenase activity IDA 11744609
GO:0004499 Function N,N-dimethylaniline monooxygenase activity IEA
GO:0005783 Component Endoplasmic reticulum IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603955 3770 ENSG00000094963
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q99518
Protein name Flavin-containing monooxygenase 2 (EC 1.14.13.-) (Dimethylaniline oxidase 2) (FMO 1B1) (Pulmonary flavin-containing monooxygenase 2) (FMO 2)
Protein function Catalyzes the oxidative metabolism of numerous xenobiotics, including mainly therapeutic drugs and insecticides that contain a soft nucleophile, most commonly nitrogen and sulfur and participates to their bioactivation (PubMed:15144220, PubMed:1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00743 FMO-like 2 → 533 Flavin-binding monooxygenase-like Family
Tissue specificity TISSUE SPECIFICITY: Expressed in lung (at protein level). Expressed predominantly in lung, and at a much lesser extent in kidney. Also expressed in fetal lung, but not in liver, kidney and brain. {ECO:0000269|PubMed:11042094, ECO:0000269|PubMed:9804831}.
Sequence
Sequence length 535
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
KEGG Pathway Reactome Pathway
Taurine and hypotaurine metabolism FMO oxidises nucleophiles
Drug metabolism - cytochrome P450  
Metabolic pathways  
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
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 Reference Evidence Score
AUTISM SPECTRUM DISORDER — CTD 35663546
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTISM SPECTRUM DISORDERS — Disgenet —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARCINOMA, BASAL CELL — CTD 36428691
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ENDOMETRIOSIS — CTD, Disgenet
CTD, Disgenet
20864642
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPEROPIA — GWAS catalog 33830181
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations