GAREM1 (GRB2 associated regulator of MAPK1 subtype 1)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 64762 |
| Gene name | GRB2 associated regulator of MAPK1 subtype 1 |
| Gene symbol | GAREM1 |
| Synonyms (NCBI Gene) |
C18orf11FAM59AGAREMGm944
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| Chromosome | 18 |
| Chromosome location | 18q12.1 |
| Summary | This gene encodes an adaptor protein which functions in the epidermal growth factor (EGF) receptor-mediated signaling pathway. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011] |
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miRNA
miRNA information provided by mirtarbase database.
1
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
14
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q9H706 | ||||||||||
| Protein name | GRB2-associated and regulator of MAPK protein 1 (GRB2-associated and regulator of MAPK1) | ||||||||||
| Protein function | [Isoform 1]: Acts as an adapter protein that plays a role in intracellular signaling cascades triggered either by the cell surface activated epidermal growth factor receptor and/or cytoplasmic protein tyrosine kinases. Promotes activation of the | ||||||||||
| PDB | 2DKZ | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Isoform 1 is ubiquitously expressed. {ECO:0000269|PubMed:19509291}. | ||||||||||
| Sequence |
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| Sequence length | 876 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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