Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2686
Gene name Gene Name - the full gene name approved by the HGNC.
Gamma-glutamyltransferase 7
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GGT7
Synonyms (NCBI Gene) Gene synonyms aliases
D20S101, GGT4, GGTL3, GGTL5
Chromosome Chromosome number
20
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
20q11.22
Summary Summary of gene provided in NCBI Entrez Gene.
This gene is a member of a gene family that encodes enzymes involved in both the metabolism of glutathione and in the transpeptidation of amino acids. Changes in the activity of gamma-glutamyltransferase may signal preneoplastic or toxic conditions in the
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT043545 hsa-miR-331-3p CLASH 23622248
MIRT611136 hsa-miR-140-3p HITS-CLIP 23824327
MIRT611136 hsa-miR-140-3p HITS-CLIP 23824327
MIRT611135 hsa-miR-6511a-3p HITS-CLIP 23824327
MIRT611134 hsa-miR-6511b-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 12270127, 25416956, 25910212, 31515488, 32296183, 33961781
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IDA 12270127
GO:0006749 Process Glutathione metabolic process IEA
GO:0006750 Process Glutathione biosynthetic process IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612342 4259 ENSG00000131067
Protein
UniProt ID Q9UJ14
Protein name Glutathione hydrolase 7 (EC 3.4.19.13) (Gamma-glutamyltransferase 7) (GGT 7) (EC 2.3.2.2) (Gamma-glutamyltransferase-like 3) (Gamma-glutamyltransferase-like 5) (Gamma-glutamyltranspeptidase 7) [Cleaved into: Glutathione hydrolase 7 heavy chain; Glutathion
Protein function Hydrolyzes and transfers gamma-glutamyl moieties from glutathione and other gamma-glutamyl compounds to acceptors.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01019 G_glu_transpept 154 655 Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed, but at low level, except in the airway epithelial cells. Detected in brain, heart, kidney, liver, lung, spleen, testis and trachea.
Sequence
Sequence length 662
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Taurine and hypotaurine metabolism
Glutathione metabolism
Metabolic pathways
  Glutathione synthesis and recycling
Aflatoxin activation and detoxification
<
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
Coronary artery disease Coronary artery disease N/A N/A GWAS
Metabolic Syndrome Metabolic syndrome N/A N/A GWAS
Myocardial Infarction Myocardial infarction N/A N/A GWAS
Neuroticism Neuroticism N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Osteoporosis Associate 27856519
Osteoporotic Fractures Associate 27856519