Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
113612
Gene name Gene Name - the full gene name approved by the HGNC.
Cytochrome P450 family 2 subfamily U member 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CYP2U1
Synonyms (NCBI Gene) Gene synonyms aliases
P450TEC, SPG49, SPG56
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q25
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This enzyme is a h
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019811 hsa-miR-375 Microarray 20215506
MIRT020782 hsa-miR-155-5p Reporter assay;Other 20584899
MIRT022645 hsa-miR-124-3p Microarray 18668037
MIRT031184 hsa-miR-19b-3p Sequencing 20371350
MIRT647217 hsa-miR-500a-5p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004497 Function Monooxygenase activity IEA
GO:0004497 Function Monooxygenase activity TAS
GO:0005506 Function Iron ion binding IEA
GO:0005737 Component Cytoplasm IBA
GO:0005739 Component Mitochondrion IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610670 20582 ENSG00000155016
Protein
UniProt ID Q7Z449
Protein name Cytochrome P450 2U1 (Long-chain fatty acid omega-monooxygenase) (EC 1.14.14.80)
Protein function A cytochrome P450 monooxygenase involved in the metabolism of arachidonic acid and its conjugates (PubMed:14660610, PubMed:24563460). Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00067 p450 101 541 Cytochrome P450 Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed with stronger expression in thymus, heart and cerebellum. {ECO:0000269|PubMed:14660610, ECO:0000269|PubMed:14975754, ECO:0000269|PubMed:15752708}.
Sequence
Sequence length 544
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Fatty acid degradation
Arachidonic acid metabolism
Metabolic pathways
  Miscellaneous substrates
Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE)
Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56)
<
Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Hereditary spastic paraplegia Hereditary spastic paraplegia, Hereditary spastic paraplegia 56 rs141431913, rs768640920, rs766380148, rs767024102, rs1248632205, rs761575210, rs397514513, rs1553937522, rs397514514, rs772400670, rs397514515 N/A
Spastic Paraplegia spastic paraplegia rs141431913, rs759033144, rs768640920, rs1578729121, rs767024102, rs397514513, rs1021034246, rs772400670 N/A
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Monoclonal Gammapathies Monoclonal gammopathy of undetermined significance N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Aicardi Goutieres syndrome Associate 23176821
Ataxia Associate 24337409
Choroidal Neovascularization Associate 34828401
Dystonia Associate 27292318
Dystonia 18 Associate 27292318
Intellectual Disability Associate 27292318
Leukoencephalopathies Associate 23176821
Macular Degeneration Associate 27292318, 34828401
Nakamura Osame syndrome Associate 23176821
Neoplastic Syndromes Hereditary Associate 24337409