GSPT2 (G1 to S phase transition 2)
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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23708 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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G1 to S phase transition 2 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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GSPT2 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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ERF3B, GST2 |
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Chromosome
Chromosome number
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X |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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Xp11.22 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a GTPase that belongs to the GTP-binding elongation factor family. The encoded protein is a polypeptide release factor that complexes with eukaryotic peptide chain release factor 1 to mediate translation termination. This protein may als |
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SNPs
SNP information provided by dbSNP.
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miRNA
miRNA 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 IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||||||||||||
| UniProt ID | Q8IYD1 | ||||||||||||||||||||
| Protein name | Eukaryotic peptide chain release factor GTP-binding subunit ERF3B (Eukaryotic peptide chain release factor subunit 3b) (eRF3b) (EC 3.6.5.-) (G1 to S phase transition protein 2 homolog) | ||||||||||||||||||||
| Protein function | GTPase component of the eRF1-eRF3-GTP ternary complex, a ternary complex that mediates translation termination in response to the termination codons UAA, UAG and UGA (PubMed:11524954, PubMed:15987998, PubMed:17562865). GSPT2/ERF3B mediates ETF1/ | ||||||||||||||||||||
| PDB | 3KUJ | ||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Highly expressed in IUCC stage II colorectal cancer (CRC). {ECO:0000269|PubMed:16721809}. | ||||||||||||||||||||
| Sequence |
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| Sequence length | 628 | ||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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