Gene Gene information from NCBI Gene database.
Entrez ID 54600
Gene name UDP glucuronosyltransferase family 1 member A9
Gene symbol UGT1A9
Synonyms (NCBI Gene)
HLUGP4LUGP4UDPGTUDPGT 1-9UGT-1IUGT1-09UGT1-9UGT1.9UGT1A9SUGT1AIUGT1I
Chromosome 2
Chromosome location 2q37.1
Summary This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a comp
miRNA miRNA information provided by mirtarbase database.
33
miRTarBase ID miRNA Experiments Reference
MIRT1473549 hsa-miR-1202 CLIP-seq
MIRT1473550 hsa-miR-136 CLIP-seq
MIRT1473551 hsa-miR-3120-5p CLIP-seq
MIRT1473552 hsa-miR-3130-3p CLIP-seq
MIRT1473553 hsa-miR-3194-5p CLIP-seq
Transcription factors Transcription factors information provided by TRRUST V2 database.
3
Transcription factor Regulation Reference
HNF1A Activation 15044625
PPARA Activation 12582161
PPARG Activation 12582161
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
38
GO ID Ontology Definition Evidence Reference
GO:0001889 Process Liver development IBA
GO:0001972 Function Retinoic acid binding IDA 20308471
GO:0004857 Function Enzyme inhibitor activity IDA 20610558
GO:0005515 Function Protein binding IPI 20610558, 27857056
GO:0005783 Component Endoplasmic reticulum IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606434 12541 ENSG00000241119
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O60656
Protein name UDP-glucuronosyltransferase 1A9 (UGT1A9) (EC 2.4.1.17) (UDP-glucuronosyltransferase 1-9) (UDPGT 1-9) (UGT1*9) (UGT1-09) (UGT1.9) (UDP-glucuronosyltransferase 1-I) (UGT-1I) (UGT1I) (lugP4)
Protein function [Isoform 1]: UDP-glucuronosyltransferase (UGT) that catalyzes phase II biotransformation reactions in which lipophilic substrates are conjugated with glucuronic acid to increase the metabolite's water solubility, thereby facilitating excretion i
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00201 UDPGT 26 521 UDP-glucoronosyl and UDP-glucosyl transferase Family
Tissue specificity TISSUE SPECIFICITY: [Isoform 1]: Expressed in liver, kidney, colon, esophagus and small intestine. {ECO:0000269|PubMed:18004212}.; TISSUE SPECIFICITY: [Isoform 2]: Expressed in liver, kidney, colon, esophagus and small intestine. {ECO:0000269|PubMed:18004
Sequence
Sequence length 530
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Pentose and glucuronate interconversions
Ascorbate and aldarate metabolism
Steroid hormone biosynthesis
Retinol metabolism
Porphyrin metabolism
Metabolism of xenobiotics by cytochrome P450
Drug metabolism - cytochrome P450
Drug metabolism - other enzymes
Metabolic pathways
Biosynthesis of cofactors
Bile secretion
Chemical carcinogenesis - DNA adducts
Chemical carcinogenesis - receptor activation
  Glucuronidation
PPARA activates gene expression
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
17
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
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BILIRUBIN METABOLISM DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CHOLELITHIASIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CRIGLER NAJJAR SYNDROME, TYPE 1 Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Breast Neoplasms Associate 22071170, 33671849, 34886806
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Associate 40026294
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 26010150
★☆☆☆☆
Found in Text Mining only
Carcinoma Non Small Cell Lung Associate 32072637
★☆☆☆☆
Found in Text Mining only
Carcinoma Renal Cell Associate 36571650
★☆☆☆☆
Found in Text Mining only
Chemical and Drug Induced Liver Injury Associate 27500989
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Associate 18675828, 24822274, 28637434, 29282011, 31698983
★☆☆☆☆
Found in Text Mining only
Death Associate 32072637
★☆☆☆☆
Found in Text Mining only
Dermatitis Atopic Associate 27549213
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Type 2 Associate 25368098
★☆☆☆☆
Found in Text Mining only