OSTF1 (osteoclast stimulating factor 1)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 26578 |
| Gene name | Osteoclast stimulating factor 1 |
| Gene symbol | OSTF1 |
| Synonyms (NCBI Gene) |
OSFSH3P2bA235O14.1
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| Chromosome | 9 |
| Chromosome location | 9q21.13 |
| Summary | Osteoclast-stimulating factor-1 is an intracellular protein produced by osteoclasts that indirectly induces osteoclast formation and bone resorption (Reddy et al., 1998 [PubMed 10092216]).[supplied by OMIM, Mar 2008] |
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miRNA
miRNA information provided by mirtarbase database.
265
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q92882 | ||||||||||||||||||||
| Protein name | Osteoclast-stimulating factor 1 | ||||||||||||||||||||
| Protein function | Induces bone resorption, acting probably through a signaling cascade which results in the secretion of factor(s) enhancing osteoclast formation and activity. | ||||||||||||||||||||
| PDB | 1X2K , 1ZLM , 3EHQ , 3EHR | ||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Ubiquitously expressed. Present in osteoclasts (at protein level). {ECO:0000269|PubMed:10092216}. | ||||||||||||||||||||
| 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 from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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