UGT1A7
UDP-glucuronosyltransferase 1A7
Also known as: UD17_HUMAN, UGT1G
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9HAW7
- Gene
- UGT1A7
- Ensembl
- ENSG00000244122
- Chromosome
- 2
- Canonical length
- 530 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins
- Quaternary structure
- Homodimer
OverviewNCBI 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 complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene has moderate glucuronidase activity with phenols. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
530 residues, UniProt reviewed canonical sequence.
>Q9HAW7|UGT1A7
1 MARAGWTGLL PLYVCLLLTC GFAKAGKLLV VPMDGSHWFT MQSVVEKLIL RGHEVVVVMP
61 EVSWQLGRSL NCTVKTYSTS YTLEDQDREF MVFADARWTA PLRSAFSLLT SSSNGIFDLF
121 FSNCRSLFND RKLVEYLKES CFDAVFLDPF DACGLIVAKY FSLPSVVFAR GIFCHYLEEG
181 AQCPAPLSYV PRLLLGFSDA MTFKERVWNH IMHLEEHLFC PYFFKNVLEI ASEILQTPVT
241 AYDLYSHTSI WLLRTDFVLE YPKPVMPNMI FIGGINCHQG KPVPMEFEAY INASGEHGIV
301 VFSLGSMVSE IPEKKAMAIA DALGKIPQTV LWRYTGTRPS NLANNTILVK WLPQNDLLGH
361 PMTRAFITHA GSHGVYESIC NGVPMVMMPL FGDQMDNAKR METKGAGVTL NVLEMTSEDL
421 ENALKAVIND KSYKENIMRL SSLHKDRPVE PLDLAVFWVE FVMRHKGAPH LRPAAHDLTW
481 YQYHSLDVIG FLLAVVLTVA FITFKCCAYG YRKCLGKKGR VKKAHKSKTHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against UGT1A7 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 79 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 79 nTPM
- vagina: 6.8 nTPM
- salivary gland: 4.8 nTPM
- tonsil: 4.8 nTPM
- skin: 3.3 nTPM
- cervix: 3 nTPM
Single-cell type
- esophageal suprabasal cells: 0.2 nCPM
- suprabasal keratinocytes: 0.2 nCPM
- basal keratinocytes: 0.1 nCPM
- esophageal apical cells: 0.1 nCPM
- esophageal basal cells: 0.1 nCPM
- adipocytes: 0 nCPM
Immune cell
- basophil: 0.2 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 6.2 nTPM
- cerebral cortex: 5.9 nTPM
- midbrain: 5.3 nTPM
- cerebellum: 5.2 nTPM
- thalamus: 5.1 nTPM
- amygdala: 4.9 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.46
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.41
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- coumarin metabolic process
- estrogen metabolic process
- fatty acid metabolic process
- flavone metabolic process
- flavonoid metabolic process
- liver development
- negative regulation of fatty acid metabolic process
- retinoic acid metabolic process
- toxin catabolic process
- xenobiotic catabolic process
- xenobiotic metabolic process
Molecular functions
- enzyme binding
- enzyme inhibitor activity
- glucuronosyltransferase activity
- protein heterodimerization activity
- protein homodimerization activity
- protein kinase C binding
- retinoic acid binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of UGT1A7 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads UGT1A7 as an antibody target. Whether an autoantibody or antibody against UGT1A7 could matter depends on whether native UGT1A7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
UGT1A7 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label UGT1A7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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