RASSF3 (Ras association domain family member 3)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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283349 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Ras association domain family member 3 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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RASSF3 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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RASSF5 |
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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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12q14.2 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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The RAS oncogene (MIM 190020) is mutated in nearly one-third of all human cancers. Members of the RAS superfamily are plasma membrane GTP-binding proteins that modulate intracellular signal transduction pathways. A subfamily of RAS effectors, including RA |
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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 | Q86WH2 | |||||||||||||||
| Protein name | Ras association domain-containing protein 3 | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Widely expressed. {ECO:0000269|PubMed:11965544}. | |||||||||||||||
| Sequence |
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| Sequence length | 238 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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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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