CHN2 (chimerin 2)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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1124 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Chimerin 2 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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CHN2 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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ARHGAP3, BCH, CHN2-3, RHOGAP3 |
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Chromosome
Chromosome number
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7 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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7p14.3 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a guanosine triphosphate (GTP)-metabolizing protein that contains a phorbol-ester/diacylglycerol (DAG)-type zinc finger, a Rho-GAP domain, and an SH2 domain. The encoded protein translocates from the cytosol to the Golgi apparatus membra |
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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 | P52757 | ||||||||||||||||||||
| Protein name | Beta-chimaerin (Beta-chimerin) (Rho GTPase-activating protein 3) | ||||||||||||||||||||
| Protein function | GTPase-activating protein for p21-rac. Insufficient expression of beta-2 chimaerin is expected to lead to higher Rac activity and could therefore play a role in the progression from low-grade to high-grade tumors. | ||||||||||||||||||||
| PDB | 1XA6 | ||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Highest levels in the brain and pancreas. Also expressed in the heart, placenta, and weakly in the kidney and liver. Expression is much reduced in the malignant gliomas, compared to normal brain or low-grade astrocytomas. | ||||||||||||||||||||
| Sequence |
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| Sequence length | 468 | ||||||||||||||||||||
| 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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