Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
54575
Gene name Gene Name - the full gene name approved by the HGNC.
UDP glucuronosyltransferase family 1 member A10
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
UGT1A10
Synonyms (NCBI Gene) Gene synonyms aliases
GNT1, UDPGT, UGT-1A, UGT-1J, UGT1, UGT1-01, UGT1-10, UGT1.1, UGT1.10, UGT1A, UGT1A1, UGT1J, hUG-BR1
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
MIRT022953 hsa-miR-124-3p Microarray 18668037
MIRT1473293 hsa-miR-1202 CLIP-seq
MIRT1473294 hsa-miR-136 CLIP-seq
MIRT1473295 hsa-miR-3120-5p CLIP-seq
MIRT1473296 hsa-miR-3130-3p CLIP-seq
Transcription factors
Transcription factor Regulation Reference
CDX2 Activation 15044625
HNF1A Activation 15044625
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001972 Function Retinoic acid binding IDA 20308471
GO:0005080 Function Protein kinase C binding IDA 18556656
GO:0005783 Component Endoplasmic reticulum IDA 17179145, 18556656
GO:0005789 Component Endoplasmic reticulum membrane TAS
GO:0015020 Function Glucuronosyltransferase activity IDA 18052087, 20056724
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606435 12531 ENSG00000242515
Protein
UniProt ID Q9HAW8
Protein name UDP-glucuronosyltransferase 1A10 (UGT1A10) (EC 2.4.1.17) (UDP-glucuronosyltransferase 1-10) (UDPGT 1-10) (UGT1*10) (UGT1-10) (UGT1.10) (UDP-glucuronosyltransferase 1-J) (UGT-1J) (UGT1J)
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: Liver and colon (PubMed:9271343). Isoform 1 and isoform 2 are expressed in colon, esophagus and small intestine; isoform 2 but not isoform 1 is expressed in liver or kidney (PubMed:18004212). {ECO:0000269|PubMed:18004212, ECO:0000269|P
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
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, 15712364, 11182932
Gilbert disease Gilbert Disease (disorder) rs72551349, rs62625011, rs34993780, rs72551351, rs748219743
Unknown
Disease term Disease name Evidence References Source
Attention Deficit Hyperactivity Disorder Attention Deficit Hyperactivity Disorder GWAS
Metabolic Syndrome Metabolic Syndrome GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Inhibit 18374377
Breast Neoplasms Associate 34886806
Carcinoma Squamous Cell Associate 10024527
Colorectal Neoplasms Associate 24822274, 31740522
Drug Related Side Effects and Adverse Reactions Associate 23160818
Environmental Illness Associate 10024527
Esophageal Squamous Cell Carcinoma Associate 10024527
Gastroschisis Associate 31075877
Neoplasms Associate 12910533, 24822274
Pancreatic Neoplasms Associate 34660806