MSANTD3-TMEFF1 (MSANTD3-TMEFF1 readthrough)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 100526694 |
| Gene name | MSANTD3-TMEFF1 readthrough |
| Gene symbol | MSANTD3-TMEFF1 |
| Synonyms (NCBI Gene) |
C9orf2C9orf3-TMEFF1C9orf30-TMEFF1H7365TMEFF1TR-1
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| Chromosome | 9 |
| Chromosome location | 9q31.1 |
| Summary | This locus represents naturally occurring read-through transcription from the neighboring MSANTD3 (Myb/SANT-like DNA-binding domain containing 3) and TMEFF1 (transmembrane protein with EGF-like and two follistatin-like domains 1) genes. The read-through t |
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miRNA
miRNA information provided by mirtarbase database.
12
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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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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