Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23708
Gene name Gene Name - the full gene name approved by the HGNC.
G1 to S phase transition 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GSPT2
Synonyms (NCBI Gene) Gene synonyms aliases
ERF3B, GST2
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xp11.22
Summary Summary of gene provided in NCBI Entrez Gene.
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
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1057519440 G>A Pathogenic Missense variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT029919 hsa-miR-26b-5p Microarray 19088304
MIRT1036326 hsa-miR-128 CLIP-seq
MIRT1036327 hsa-miR-129-5p CLIP-seq
MIRT1036328 hsa-miR-144 CLIP-seq
MIRT1036329 hsa-miR-27a CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000184 Process Nuclear-transcribed mRNA catabolic process, nonsense-mediated decay TAS
GO:0002184 Process Cytoplasmic translational termination IBA 21873635
GO:0003723 Function RNA binding HDA 22658674, 22681889
GO:0003747 Function Translation release factor activity IBA 21873635
GO:0003924 Function GTPase activity IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
300418 4622 ENSG00000189369
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

Accession ID Position in sequence Description Type
PF07145 PAM2 47 64 Ataxin-2 C-terminal region Motif
PF00009 GTP_EFTU 201 478 Elongation factor Tu GTP binding domain Domain
PF03143 GTP_EFTU_D3 516 624 Elongation factor Tu C-terminal domain Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in IUCC stage II colorectal cancer (CRC). {ECO:0000269|PubMed:16721809}.
Sequence
Sequence length 628
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  mRNA surveillance pathway   Eukaryotic Translation Termination
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Autism Autistic Disorder rs121964908, rs62643608, rs181327458, rs797046134, rs869312704, rs1555013332, rs876657679, rs1057518999, rs1057518658, rs771827120, rs1555187899, rs773080572, rs753871454, rs1684130791, rs1684180699
View all (8 more)
Unknown
Disease term Disease name Evidence References Source
Mental retardation intellectual disability GenCC
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 24466059
Developmental Disabilities Associate 28414775
Hepatitis B Associate 30867251
Hepatitis B Chronic Associate 24466059
Intellectual Disability Associate 20655035, 28414775
Joint Instability Associate 28414775
Lymphoproliferative Syndrome X Linked 2 Associate 28414775
Megalencephaly Associate 28414775
Muscle Hypotonia Associate 28414775
Neoplasms Associate 30867251