Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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2953 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Glutathione S-transferase theta 2 (gene/pseudogene) |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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GSTT2 |
SynonymsGene synonyms aliases
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- |
ChromosomeChromosome number
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22 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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22q11.23 |
SummarySummary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene, glutathione S-transferase (GST) theta 2 (GSTT2), is a member of a superfamily of proteins that catalyze the conjugation of reduced glutathione to a variety of electrophilic and hydrophobic compounds. Human GSTs can be div |
miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
P0CG29 |
Protein name |
Glutathione S-transferase theta-2 (EC 2.5.1.18) (GST class-theta-2) |
Protein function |
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles (PubMed:1417752). Has a sulfatase activity (PubMed:1417752). |
PDB |
4MPF
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Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF02798 |
GST_N |
5 → 75 |
Glutathione S-transferase, N-terminal domain |
Domain |
PF00043 |
GST_C |
86 → 199 |
Glutathione S-transferase, C-terminal domain |
Domain |
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Sequence |
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Sequence length |
244 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Facioscapulohumeral muscular dystrophy |
Muscular Dystrophy, Facioscapulohumeral |
rs387907319, rs397514623, rs1057519614, rs1598416221, rs886041918, rs886042417, rs1057519644, rs1245372794, rs1555642277, rs1555644339, rs1555647265, rs886044369, rs1568350731, rs377471712, rs2075161300, rs2075566961, rs2075161499 |
12868502 |
Hypertension |
Hypertensive disease |
rs13306026, rs13333226 |
22228705 |
Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
19528963 |
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