GRIP1 (glutamate receptor interacting protein 1)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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23426 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Glutamate receptor interacting protein 1 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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GRIP1 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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FRASRS3, GRIP |
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Chromosome
Chromosome number
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12 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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12q14.3 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of the glutamate receptor interacting protein family. The encoded scaffold protein binds to and mediates the trafficking and membrane organization of a number of transmembrane proteins. Alternatively spliced transcript variants |
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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 | Q9Y3R0 | ||||||||||||||||||||||||||||||||||||||||
| Protein name | Glutamate receptor-interacting protein 1 (GRIP-1) | ||||||||||||||||||||||||||||||||||||||||
| Protein function | May play a role as a localized scaffold for the assembly of a multiprotein signaling complex and as mediator of the trafficking of its binding partners at specific subcellular location in neurons (PubMed:10197531). Through complex formation with | ||||||||||||||||||||||||||||||||||||||||
| PDB | 2JIL | ||||||||||||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 1128 | ||||||||||||||||||||||||||||||||||||||||
| 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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