ZNF365 (zinc finger protein 365)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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22891 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Zinc finger protein 365 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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ZNF365 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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Su48, UAN, ZNF365D |
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Chromosome
Chromosome number
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10 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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10q21.2 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a zinc finger protein that may play a role in the repair of DNA damage and maintenance of genome stability. The N-terminal C2H2 zinc finger motif is required to form a protein complex with PARP1 and MRE11, which are known to be involved |
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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 | Q70YC4 | |
| Protein name | Talanin | |
| Protein function | May play a role in uric acid excretion. | |
| Family and domains | ||
| Tissue specificity | TISSUE SPECIFICITY: Isoform 4 is expressed in placenta, lung, kidney and pancreas. {ECO:0000269|PubMed:12740763}. | |
| Sequence |
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| Sequence length | 216 | |
| UniProt ID | Q70YC5 | |
| Protein name | Protein ZNF365 (DISC1-binding zinc-finger protein) (Protein su48) | |
| Protein function | Involved in the regulation of neurogenesis. Negatively regulates neurite outgrowth (PubMed:17389905). Involved in the morphogenesis of basket cells in the somatosensory cortex during embryogenesis. Involved in the positive regulation of oligoden | |
| Family and domains | ||
| Tissue specificity | TISSUE SPECIFICITY: Isoform 1 is expressed in brain. Isoform 2 is expressed in placenta and at low level in lung and liver. Isoform 3 is expressed in kidney and pancreas. Isoform 1 is expressed exclusively in brain (PubMed:17389905). {ECO:0000269|PubMed:1 | |
| Sequence |
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| Sequence length | 407 | |
| Interactions | View interactions | |
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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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