MYL12BP2 (MYL12B pseudogene 2)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 391722 |
| Gene name | MYL12B pseudogene 2 |
| Gene symbol | MYL12BP2 |
| Synonyms (NCBI Gene) |
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| Chromosome | 4 |
| Chromosome location | 4q35.1 |
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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.).
5
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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 MYL12BP2 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to MYL12BP2 (see Related Genes above), that are NOT already directly curated for MYL12BP2 itself -- a lead worth checking, not a confirmed association.
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