Gene Gene information from NCBI Gene database.
Entrez ID 1551
Gene name Cytochrome P450 family 3 subfamily A member 7
Gene symbol CYP3A7
Synonyms (NCBI Gene)
CP37CYPIIIA7P-450(HFL33)P-450111A7P450-HFLAP450HLp2
Chromosome 7
Chromosome location 7q22.1
Summary This gene encodes a member of the cytochrome P450 superfamily of enzymes, which participate in drug metabolism and the synthesis of cholesterol, steroids and other lipids. This enzyme hydroxylates testosterone and dehydroepiandrosterone 3-sulphate, which
miRNA miRNA information provided by mirtarbase database.
29
miRTarBase ID miRNA Experiments Reference
MIRT921557 hsa-miR-103a CLIP-seq
MIRT921558 hsa-miR-107 CLIP-seq
MIRT921559 hsa-miR-1208 CLIP-seq
MIRT921560 hsa-miR-1255a CLIP-seq
MIRT921561 hsa-miR-1255b CLIP-seq
Transcription factors Transcription factors information provided by TRRUST V2 database.
7
Transcription factor Regulation Reference
FOXA3 Unknown 19706729
NFAT5 Unknown 17600221
NFKB1 Unknown 19928584
RELA Unknown 19928584
SP1 Unknown 11495920
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
34
GO ID Ontology Definition Evidence Reference
GO:0002933 Process Lipid hydroxylation IDA 14559847
GO:0004497 Function Monooxygenase activity IEA
GO:0004497 Function Monooxygenase activity ISS
GO:0004497 Function Monooxygenase activity TAS
GO:0005506 Function Iron ion binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605340 2640 ENSG00000160870
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Steroid hormone biosynthesis
Retinol metabolism
Metabolic pathways
Chemical carcinogenesis - DNA adducts
  Xenobiotics
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
AUTISM SPECTRUM DISORDER CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GOUT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Adrenal Gland Neoplasms Associate 18445661
★☆☆☆☆
Found in Text Mining only
Anencephaly Associate 15845858
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Associate 26964624, 33495599
★☆☆☆☆
Found in Text Mining only
Calcinosis Cutis Inhibit 22971343
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Associate 40026294
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 25024626, 25101946
★☆☆☆☆
Found in Text Mining only
Carcinoma Renal Cell Associate 32789468
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Associate 23036011
★☆☆☆☆
Found in Text Mining only
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Associate 21915484
★☆☆☆☆
Found in Text Mining only
Drug Related Side Effects and Adverse Reactions Associate 26964624
★☆☆☆☆
Found in Text Mining only