Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
54579
Gene name Gene Name - the full gene name approved by the HGNC.
UDP glucuronosyltransferase family 1 member A5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
UGT1A5
Synonyms (NCBI Gene) Gene synonyms aliases
UDPGT, UDPGT 1-5, UGT1E
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
MIRT1473421 hsa-miR-1202 CLIP-seq
MIRT1473422 hsa-miR-136 CLIP-seq
MIRT1473423 hsa-miR-3120-5p CLIP-seq
MIRT1473424 hsa-miR-3130-3p CLIP-seq
MIRT1473425 hsa-miR-3194-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005789 Component Endoplasmic reticulum membrane IEA
GO:0015020 Function Glucuronosyltransferase activity IEA
GO:0016021 Component Integral component of membrane IEA
GO:0052696 Process Flavonoid glucuronidation IBA 21873635
GO:0052697 Process Xenobiotic glucuronidation IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606430 12537 ENSG00000288705
Protein
UniProt ID P35504
Protein name UDP-glucuronosyltransferase 1A5 (UGT1A5) (EC 2.4.1.17) (UDP-glucuronosyltransferase 1-5) (UDPGT 1-5) (UGT1*5) (UGT1-05) (UGT1.5) (UDP-glucuronosyltransferase 1-E) (UGT-1E) (UGT1E)
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 29 525 UDP-glucoronosyl and UDP-glucosyl transferase Family
Tissue specificity TISSUE SPECIFICITY: Isoform 1 and isoform 2 are expressed in colon and small intestine. Neither isoform is expressed in liver, kidney or esophagus. {ECO:0000269|PubMed:18004212}.
Sequence
Sequence length 534
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
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Anemia Anemia, Sickle Cell rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966
View all (89 more)
22558097
Cholelithiasis Cholelithiasis rs121918440, rs72552778, rs387906528, rs759202962, rs377160065, rs1051861187, rs757693457, rs752563752 22558097
Crigler-najjar syndrome Crigler Najjar syndrome, type 1, Crigler Najjar syndrome, type 2 rs587776761, rs72551353, rs111033539, rs72551349, rs72551348, rs587776762, rs62625011, rs281865418, rs587776763, rs587776764, rs587776765, rs587776766, rs34993780, rs72551351, rs111033541
View all (7 more)
26697581, 11182932, 15712364
Gilbert disease Gilbert Disease (disorder) rs72551349, rs62625011, rs34993780, rs72551351, rs748219743
Unknown
Disease term Disease name Evidence References Source
Metabolic Syndrome Metabolic Syndrome GWAS
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 37622118
Gastroschisis Associate 31075877
Neoplasms Associate 23468910
Stomach Neoplasms Associate 25712374