RHOJ (ras homolog family member J)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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57381 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Ras homolog family member J |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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RHOJ |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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ARHJ, RASL7B, TC10B, TCL |
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Chromosome
Chromosome number
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14 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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14q23.2 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes one of the many small GTP-binding proteins in the Rho family shown to be associated with focal adhesions in endothelial cells (PMID: 21148427, 22103495). The encoded protein is activated by vascular endothelial growth factor and may regu |
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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 | Q9H4E5 | ||||||||||
| Protein name | Rho-related GTP-binding protein RhoJ (Ras-like protein family member 7B) (Tc10-like GTP-binding protein) | ||||||||||
| Protein function | Plasma membrane-associated small GTPase specifically involved in angiogenesis (PubMed:21628409, PubMed:24434213, PubMed:30158707). Required for endothelial cell migration during vascular development via its interaction with GLUL (PubMed:30158707 | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Specifically expressed in endothelial cells in different tissues, such as brain, heart, lung and liver. {ECO:0000269|PubMed:21628409}. | ||||||||||
| Sequence |
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| Sequence length | 214 | ||||||||||
| 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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