CYP2A13 (cytochrome P450 family 2 subfamily A member 13)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 1553 |
| Gene name | Cytochrome P450 family 2 subfamily A member 13 |
| Gene symbol | CYP2A13 |
| Synonyms (NCBI Gene) |
CPADCYP2ACYPIIA13
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| Chromosome | 19 |
| Chromosome location | 19q13.2 |
| Summary | 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 protein local |
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miRNA
miRNA information provided by mirtarbase database.
5
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
24
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q16696 | ||||||||||
| Protein name | Cytochrome P450 2A13 (EC 1.14.14.1) (CYPIIA13) | ||||||||||
| Protein function | Exhibits a coumarin 7-hydroxylase activity. Active in the metabolic activation of hexamethylphosphoramide, N,N-dimethylaniline, 2'-methoxyacetophenone, N-nitrosomethylphenylamine, and the tobacco-specific carcinogen, 4-(methylnitrosamino)-1-(3-p | ||||||||||
| PDB | 2P85 , 2PG5 , 2PG6 , 2PG7 , 3T3S , 4EJG , 4EJH , 4EJI | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed in liver and a number of extrahepatic tissues, including nasal mucosa, lung, trachea, brain, mammary gland, prostate, testis, and uterus, but not in heart, kidney, bone marrow, colon, small intestine, spleen, stomach, thymus, | ||||||||||
| Sequence |
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| Sequence length | 494 | ||||||||||
| Interactions | View interactions | ||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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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)
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