SH3RF1 (SH3 domain containing ring finger 1)
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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57630 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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SH3 domain containing ring finger 1 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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SH3RF1 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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POSH, RNF142, SH3MD2 |
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Chromosome
Chromosome number
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4 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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4q32.3-q33 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a protein containing an N-terminus RING-finger, four SH3 domains, and a region implicated in binding of the Rho GTPase Rac. Via the RING-finger, the encoded protein has been shown to function as an ubiquitin-protein ligase involved in pr |
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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 | Q7Z6J0 | ||||||||||||||||||||||||||||||
| Protein name | E3 ubiquitin-protein ligase SH3RF1 (EC 2.3.2.27) (Plenty of SH3s) (Protein POSH) (RING finger protein 142) (RING-type E3 ubiquitin transferase SH3RF1) (SH3 domain-containing RING finger protein 1) (SH3 multiple domains protein 2) | ||||||||||||||||||||||||||||||
| Protein function | Has E3 ubiquitin-protein ligase activity. In the absence of an external substrate, it can catalyze self-ubiquitination (PubMed:15659549, PubMed:20696164). Stimulates ubiquitination of potassium channel KCNJ1, enhancing it's dynamin-dependent and | ||||||||||||||||||||||||||||||
| PDB | 7NZC , 7NZD | ||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 888 | ||||||||||||||||||||||||||||||
| 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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