FAM9A (family with sequence similarity 9 member A)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 171482 |
| Gene name | Family with sequence similarity 9 member A |
| Gene symbol | FAM9A |
| Synonyms (NCBI Gene) |
TEX39A
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| Chromosome | X |
| Chromosome location | Xp22.31 |
| Summary | This gene is a member of a gene family which arose through duplication on the X chromosome. The encoded protein may be a nuclear protein that is localized to the nucleolus, and has some similarity to a synaptonemal complex protein. Multiple alternatively |
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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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Q8IZU1 |
| Protein name | Protein FAM9A |
| Family and domains | |
| Tissue specificity | TISSUE SPECIFICITY: Expressed exclusively in testis. {ECO:0000269|PubMed:12213195}. |
| Sequence |
MEPVGRKRSRKAAKAQLEAQVTAAQGATKEGSGIASNFPGQPTMEPVGRKRSRKAAKAQL |
| Sequence length | 332 |
| Interactions | View interactions |
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Related Genes
Genes most often co-reported with FAM9A across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to FAM9A (see Related Genes above), that are NOT already directly curated for FAM9A itself -- a lead worth checking, not a confirmed association.
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