MAGEA8 (MAGE family member A8)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 4107 |
| Gene name | MAGE family member A8 |
| Gene symbol | MAGEA8 |
| Synonyms (NCBI Gene) |
CT1.8MAGE8
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| Chromosome | X |
| Chromosome location | Xq28 |
| Summary | This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of thi |
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miRNA
miRNA information provided by mirtarbase database.
4
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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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P43361 | |||||||||||||||
| Protein name | Melanoma-associated antigen 8 (Cancer/testis antigen 1.8) (CT1.8) (MAGE-8 antigen) | |||||||||||||||
| Protein function | Not known, though may play a role in embryonal development and tumor transformation or aspects of tumor progression. | |||||||||||||||
| PDB | 8FJB | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed in many tumors of several types, such as melanoma, head and neck squamous cell carcinoma, lung carcinoma and breast carcinoma, but not in normal tissues except for testis and placenta. | |||||||||||||||
| Sequence | ||||||||||||||||
| Sequence length | 318 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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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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