RRAGB (Ras related GTP binding B)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 10325 |
| Gene name | Ras related GTP binding B |
| Gene symbol | RRAGB |
| Synonyms (NCBI Gene) |
RAGBbA465E19.1
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| Chromosome | X |
| Chromosome location | Xp11.21 |
| Summary | Ras-homologous GTPases constitute a large family of signal transducers that alternate between an activated, GTP-binding state and an inactivated, GDP-binding state. These proteins represent cellular switches that are operated by GTP-exchange factors and f |
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miRNA
miRNA information provided by mirtarbase database.
7
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
35
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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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Q5VZM2 | ||||||||||
| Protein name | Ras-related GTP-binding protein B (Rag B) (RagB) (EC 3.6.5.-) | ||||||||||
| Protein function | Guanine nucleotide-binding protein that plays a crucial role in the cellular response to amino acid availability through regulation of the mTORC1 signaling cascade (PubMed:18497260, PubMed:20381137, PubMed:23723238, PubMed:24095279). Forms heter | ||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 374 | ||||||||||
| 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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