LYNX1-SLURP2 (LYNX1-SLURP2 readthrough)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 111188157 |
| Gene name | LYNX1-SLURP2 readthrough |
| Gene symbol | LYNX1-SLURP2 |
| Synonyms (NCBI Gene) |
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| Chromosome | 8 |
| Chromosome location | 8q24.3 |
| Summary | This locus represents naturally occurring read-through transcription between the neighboring LYNX1 and SLURP2 genes. The readthrough transcript encodes a fusion protein comprised of sequence sharing identity with each individual gene product. The signific |
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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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