ZNF687 (zinc finger protein 687)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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57592 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Zinc finger protein 687 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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ZNF687 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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PDB6 |
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Chromosome
Chromosome number
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1 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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1q21.3 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes C2H2 zinc finger protein. The encoded protein may play a role in bone differentiation and development. Mutations in this gene are the cause of Paget disease of bone-6. Alternate splicing results in multiple transcript variants. [provided |
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SNPs
SNP information provided by dbSNP.
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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 | Q8N1G0 | ||||||||||||||||||||
| Protein name | Zinc finger protein 687 | ||||||||||||||||||||
| Protein function | May be involved in transcriptional regulation. | ||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Widely expressed with highest levels in obvary, muscle, blood and lung. {ECO:0000269|PubMed:26849110}. | ||||||||||||||||||||
| Sequence |
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| Sequence length | 1237 | ||||||||||||||||||||
| 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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