RANGRF (RAN guanine nucleotide release factor)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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29098 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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RAN guanine nucleotide release factor |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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RANGRF |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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HSPC165, HSPC236, MOG1, RANGNRF |
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Chromosome
Chromosome number
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17 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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17p13.1 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a protein that has been shown to function as a guanine nucleotide release factor in mouse and to regulate the expression and function of the Nav1.5 cardiac sodium channel in human. Alternative splicing results in multiple transcript vari |
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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 | Q9HD47 | ||||||||||
| Protein name | Ran guanine nucleotide release factor (RanGNRF) (Ran-binding protein MOG1) | ||||||||||
| Protein function | May regulate the intracellular trafficking of RAN (PubMed:11290418). Promotes guanine nucleotide release from RAN and inhibits binding of new GTP by preventing the binding of the RAN guanine nucleotide exchange factor RCC1 (PubMed:29040603). Reg | ||||||||||
| PDB | 5YFG | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Isoform 1 and isoform 2 are ubiquitously expressed (PubMed:11290418). Detected in heart and brain (PubMed:21621375). {ECO:0000269|PubMed:11290418, ECO:0000269|PubMed:21621375}. | ||||||||||
| Sequence |
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| Sequence length | 186 | ||||||||||
| 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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