GRAP2 (GRB2 related adaptor protein 2)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 9402 |
| Gene name | GRB2 related adaptor protein 2 |
| Gene symbol | GRAP2 |
| Synonyms (NCBI Gene) |
GADSGRAP-2GRB2LGRBLGGRIDGRPLGrbXGrf40MonaP38
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| Chromosome | 22 |
| Chromosome location | 22q13.1 |
| Summary | This gene encodes a member of the GRB2/Sem5/Drk family. This member is an adaptor-like protein involved in leukocyte-specific protein-tyrosine kinase signaling. Like its related family member, GRB2-related adaptor protein (GRAP), this protein contains an |
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miRNA
miRNA information provided by mirtarbase database.
85
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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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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O75791 | ||||||||||||||||||||
| Protein name | GRB2-related adapter protein 2 (Adapter protein GRID) (GRB-2-like protein) (GRB2L) (GRBLG) (GRBX) (Grf40 adapter protein) (Grf-40) (Growth factor receptor-binding protein) (Hematopoietic cell-associated adapter protein GrpL) (P38) (Protein GADS) (SH3-SH2- | ||||||||||||||||||||
| Protein function | Interacts with SLP-76 to regulate NF-AT activation. Binds to tyrosine-phosphorylated shc. | ||||||||||||||||||||
| PDB | 5GJH | ||||||||||||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 330 | ||||||||||||||||||||
| 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 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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