RHPN2 (rhophilin Rho GTPase binding protein 2)
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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85415 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Rhophilin Rho GTPase binding protein 2 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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RHPN2 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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P76RBE, RHOBP |
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Chromosome
Chromosome number
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19 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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19q13.11 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of the rhophilin family of Ras-homologous (Rho)-GTPase binding proteins. The encoded protein binds both GTP- and GDP-bound RhoA and GTP-bound RhoB and may be involved in the organization of the actin cytoskeleton. [provided by R |
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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 | Q8IUC4 | |||||||||||||||
| Protein name | Rhophilin-2 (76 kDa RhoB effector protein) (GTP-Rho-binding protein 2) (p76RBE) | |||||||||||||||
| Protein function | Binds specifically to GTP-Rho. May function in a Rho pathway to limit stress fiber formation and/or increase the turnover of F-actin structures in the absence of high levels of RhoA activity. | |||||||||||||||
| PDB | 2VSV | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Widely expressed. Highly expressed in prostate, trachea, stomach, colon, thyroid and pancreas. Expressed at lower level in brain, spinal cord, kidney, placenta and liver. {ECO:0000269|PubMed:12221077, ECO:0000269|PubMed:12473120}. | |||||||||||||||
| Sequence |
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| Sequence length | 686 | |||||||||||||||
| 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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