AFM (afamin)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 173 |
| Gene name | Afamin |
| Gene symbol | AFM |
| Synonyms (NCBI Gene) |
ALB2ALBAALF
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| Chromosome | 4 |
| Chromosome location | 4q13.3 |
| Summary | This gene is a member of the albumin gene family, which is comprised of four genes that localize to chromosome 4 in a tandem arrangement. These four genes encode structurally-related serum transport proteins that are known to be evolutionarily related. Th |
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
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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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P43652 | ||||||||||||||||||||
| Protein name | Afamin (Alpha-albumin) (Alpha-Alb) | ||||||||||||||||||||
| Protein function | Functions as a carrier for hydrophobic molecules in body fluids (Probable). Essential for the solubility and activity of lipidated Wnt family members, including WNT1, WNT2B, WNT3, WNT3A, WNT5A, WNT7A, WNT7B, WNT8, WNT9A, WNT9B, WNT10A and WNT10B | ||||||||||||||||||||
| PDB | 5OKL , 6FAK , 6RQ7 | ||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: High level detected in plasma but also in extravascular fluids such as follicular and cerebrospinal fluids (at protein level). {ECO:0000269|PubMed:12463752, ECO:0000269|PubMed:15952736, ECO:0000269|PubMed:7517938}. | ||||||||||||||||||||
| Sequence | |||||||||||||||||||||
| Sequence length | 599 | ||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||