Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
54600
Gene name Gene Name - the full gene name approved by the HGNC.
UDP glucuronosyltransferase family 1 member A9
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
UGT1A9
Synonyms (NCBI Gene) Gene synonyms aliases
HLUGP4, LUGP4, UDPGT, UDPGT 1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1A9S, UGT1AI, UGT1I
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q37.1
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 factor Regulation Reference
HNF1A Activation 15044625
PPARA Activation 12582161
PPARG Activation 12582161
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606434 12541 ENSG00000241119
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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
Attention Deficit Hyperactivity Disorder Attention deficit hyperactivity disorder N/A N/A GWAS
Cholelithiasis Cholelithiasis N/A N/A GWAS
Metabolic Syndrome Serum bilirubin levels in metabolic syndrome N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 22071170, 33671849, 34886806
Carcinogenesis Associate 40026294
Carcinoma Hepatocellular Associate 26010150
Carcinoma Non Small Cell Lung Associate 32072637
Carcinoma Renal Cell Associate 36571650
Chemical and Drug Induced Liver Injury Associate 27500989
Colorectal Neoplasms Associate 18675828, 24822274, 28637434, 29282011, 31698983
Death Associate 32072637
Dermatitis Atopic Associate 27549213
Diabetes Mellitus Type 2 Associate 25368098