Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6002
Gene name Gene Name - the full gene name approved by the HGNC.
Regulator of G protein signaling 12
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RGS12
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4p16.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the `regulator of G protein signaling` (RGS) gene family. The encoded protein may function as a guanosine triphosphatase (GTPase)-activating protein as well as a transcriptional repressor. This protein may play a role in tumo
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT045830 hsa-miR-138-5p CLASH 23622248
MIRT045473 hsa-miR-149-5p CLASH 23622248
MIRT716003 hsa-miR-4459 HITS-CLIP 19536157
MIRT716002 hsa-miR-665 HITS-CLIP 19536157
MIRT716001 hsa-miR-6840-3p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000794 Component Condensed nuclear chromosome TAS 10869340
GO:0003924 Function GTPase activity TAS
GO:0005096 Function GTPase activator activity IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602512 9994 ENSG00000159788
Protein
UniProt ID O14924
Protein name Regulator of G-protein signaling 12 (RGS12)
Protein function Regulates G protein-coupled receptor signaling cascades. Inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits, thereby driving them into their inactive GDP-bound form. ; FUNCTI
PDB 2EBZ , 2KV8
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00595 PDZ 22 96 PDZ domain Domain
PF00615 RGS 715 831 Regulator of G protein signaling domain Domain
PF16613 RGS12_us1 836 953 Disordered
PF02196 RBD 963 1030 Raf-like Ras-binding domain Domain
PF02196 RBD 1034 1102 Raf-like Ras-binding domain Domain
PF16611 RGS12_us2 1106 1180 Disordered
PF02188 GoLoco 1188 1209 GoLoco motif Motif
PF16612 RGS12_usC 1239 1376 Disordered
Tissue specificity TISSUE SPECIFICITY: Isoform 3 is brain specific.
Sequence
MFRAGEASKRPLPGPSPPRVRSVEVARGRAGYGFTLSGQAPCVLSCVMRGSPADFVGLRA
GDQILAVNEINVKKASHEDVVKLIGKCSGVLHMVIA
EGVGRFESCSSDEEGGLYEGKGWL
KPKLDSKALGINRAERVVEEMQSGGIFNMIFENPSLCASNSEPLKLKQRSLSESAATRFD
VGHESINNPNPNMLSKEEISKVIHDDSVFSIGLESHDDFALDASILNVAMIVGYLGSIEL
PSTSSNLESDSLQAIRGCMRRLRAEQKIHSLVTMKIMHDCVQLSTDKAGVVAEYPAEKLA
FSAVCPDDRRFFGLVTMQTNDDGSLAQEEEGALRTSCHVFMVDPDLFNHKIHQGIARRFG
FECTADPDTNGCLEFPASSLPVLQFISVLYRDMGELIEGMRARAFLDGDADAHQNNSTSS
NSDSGIGNFHQEEKSNRVLVVDLGGSSSRHGPGGSAWDGVGGRGAQPWGAPWTGPFCPDP
EGSPPFEAAHQTDRFWDLNKHLGPASPVEVPPASLRSSVPPSKRGTVGAGCGFNQRWLPV
HVLREWQCGHTSDQDSYTDSTDGWSSINCGTLPPPMSKIPADRYRVEGSFAQPPLNAPKR
EWSRKAFGMQSIFGPHRNVRKTKEDKKGSKFGRGTGLTQPSQRTSARRSFGRSKRFSITR
SLDDLESATVSDGELTGADLKDCVSNNSLSSNASLPSVQSCRRLRERRVASWAVSFERLL
QDPVGVRYFSDFLRKEFSEENILFWQACEYFNHVPAHDKKELSYRAREIFSKFLCSKATT
PVNIDSQAQLADDVLRAPHPDMFKEQQLQIFNLMKFDSYTRFLKSPLYQEC
ILAEVEGRA
LPDSQQVPSSPASKHSLGSDHSSVSTPKKLSGKSKSGRSLNEELGDEDSEKKRKGAFFSW
SRTRSTGRSQKKREHGDHADDALHANGGLCRRESQGSVSSAGSLDLSEACRTL
APEKDKA
TKHCCIHLPDGTSCVVAVKAGFSIKDILSGLCERHGINGAAADLFLVGGDKPLVLHQDSS
ILESRDLRLE
KRTLFRLDLVPINRSVGLKAKPTKPVTEVLRPVVARYGLDLSGLLVRLSG
EKEPLDLGAPISSLDGQRVVLE
EKDPSRGKASADKQKGVPVKQNTAVNSSSRNHSATGEE
RTLGKSNSIKIKGENGKNARDPRLSKREESIAKIGKKKYQ
KINLDEAEEFFELISKAQSN
RADDQRGLL
RKEDLVLPEFLRLPPGSTELTLPTPAAVAKGFSKRSATGNGRESASQPGEQ
WEPVQESSDSPSTSPGSASSPPGPPGTTPPGQKSPSGPFCTPQSPVSLAQEGTAQIWKRQ
SQEVEAGGIQTVEDEHVAELTLMGEGDISSPNSTLLPPPSTPQEVPGPSRPGSGTH
GSRD
LPVNRIIDVDLVTGSAPGRDGGIAGAQAGPGRSQASGGPPTSDLPGLGPVPGEPAKPKTS
AHHATFV
Sequence length 1447
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    G alpha (i) signalling events
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
21822266
Unknown
Disease term Disease name Evidence References Source
Huntington disease Huntington Disease 22387017 ClinVar
Myocardial infarction Myocardial Infarction 21211798 ClinVar
Metabolic Syndrome Metabolic Syndrome GWAS
Dementia Dementia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Arthritis Rheumatoid Associate 25848939
Bipolar Disorder Associate 32066727, 39518985
Breast Neoplasms Associate 28798985
Carcinoma Hepatocellular Stimulate 35068348
Carcinoma Non Small Cell Lung Associate 21698121
Colorectal Neoplasms Associate 21209843
Fibrocystic Breast Disease Associate 28798985
Heart Diseases Associate 35748249
Schizophrenia Associate 25420024
Stomach Neoplasms Associate 34034702