TRIM39-RPP21 (TRIM39-RPP21 readthrough)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 202658 |
| Gene name | TRIM39-RPP21 readthrough |
| Gene symbol | TRIM39-RPP21 |
| Synonyms (NCBI Gene) |
TRIM39R
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| Chromosome | 6 |
| Chromosome location | 6p22.1 |
| Summary | This locus represents naturally occurring read-through transcription between the neighboring TRIM39 (tripartite motif-containing 39) and RPP21 (ribonuclease P/MRP 21kDa subunit) genes on chromosome 6. The read-through transcript encodes a fusion protein t |
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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.).
7
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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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Related Genes
Genes most often co-reported with TRIM39-RPP21 across shared curated disease and pathway associations.
3
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to TRIM39-RPP21 (see Related Genes above), that are NOT already directly curated for TRIM39-RPP21 itself -- a lead worth checking, not a confirmed association.
5
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