Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6000
Gene name Gene Name - the full gene name approved by the HGNC.
Regulator of G protein signaling 7
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RGS7
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q43|1q23.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1304542 hsa-miR-1 CLIP-seq
MIRT1304543 hsa-miR-206 CLIP-seq
MIRT1304544 hsa-miR-3166 CLIP-seq
MIRT1304545 hsa-miR-329 CLIP-seq
MIRT1304546 hsa-miR-362-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001965 Function G-protein alpha-subunit binding IDA 36996198
GO:0003924 Function GTPase activity IEA
GO:0003924 Function GTPase activity TAS
GO:0005096 Function GTPase activator activity IBA
GO:0005096 Function GTPase activator activity IDA 10521509, 31189666, 36996198
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602517 10003 ENSG00000182901
Protein
UniProt ID P49802
Protein name Regulator of G-protein signaling 7 (RGS7)
Protein function GTPase activator component of the RGS7-GNB5 complex that regulates G protein-coupled receptor signaling cascades (PubMed:10521509, PubMed:10862767, PubMed:31189666). The RGS7-GNB5 complex acts as an inhibitor signal transduction by promoting the
PDB 2A72 , 2D9J , 7EWP , 7EWR , 7SHF
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00610 DEP 40 110 Domain found in Dishevelled, Egl-10, and Pleckstrin (DEP) Domain
PF18148 RGS_DHEX 113 214 Regulator of G-protein signalling DHEX domain Domain
PF00631 G-gamma 252 316 GGL domain Domain
PF00615 RGS 333 447 Regulator of G protein signaling domain Domain
Sequence
Sequence length 495
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    G alpha (i) signalling events
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding
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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
Dementia Dementia N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS
Mental Depression Major depressive disorder N/A N/A GWAS
Metabolic Syndrome Metabolic syndrome N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 37761960
Carcinoma Non Small Cell Lung Associate 21698121
Cerebral Infarction Associate 27533483
Cognition Disorders Associate 25712083
Congenital Hereditary and Neonatal Diseases and Abnormalities Associate 25712083
Hypertriglyceridemia Associate 39662927
Inflammation Associate 36999276
Melanoma Associate 29330521
Neoplasms Associate 23555580
Neoplasms Inhibit 29330521