Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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6002 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Regulator of G protein signaling 12 |
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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RGS12 |
SynonymsGene synonyms aliases
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- |
ChromosomeChromosome number
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4 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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4p16.3 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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 |
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
|
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 |
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Disordered |
PF02188 |
GoLoco |
1188 → 1209 |
GoLoco motif |
Motif |
PF16612 |
RGS12_usC |
1239 → 1376 |
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Disordered |
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Sequence |
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Sequence length |
1447 |
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 |
Myocardial infarction |
Myocardial Infarction |
rs12316150, rs41303970, rs909253, rs7291467, rs2234693 |
21211798 |
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 |
21822266 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Huntington disease |
Huntington Disease |
rs768047421 |
22387017 |
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