FGF20 (fibroblast growth factor 20)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 26281 |
| Gene name | Fibroblast growth factor 20 |
| Gene symbol | FGF20 |
| Synonyms (NCBI Gene) |
FGF-20RHDA2
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| Chromosome | 8 |
| Chromosome location | 8p22 |
| Summary | The protein encoded by this gene is a member of the fibroblast growth factor family. The fibroblast growth factors possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes including embryonic development, |
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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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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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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Q9NP95 | ||||||||||
| Protein name | Fibroblast growth factor 20 (FGF-20) | ||||||||||
| Protein function | Neurotrophic factor that regulates central nervous development and function. | ||||||||||
| PDB | 3F1R | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Predominantly expressed in the cerebellum. {ECO:0000269|PubMed:11306498}. | ||||||||||
| Sequence |
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| Sequence length | 211 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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