GCOM1 (GCOM1, MYZAP-POLR2M combined locus)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 145781 |
| Gene name | GCOM1, MYZAP-POLR2M combined locus |
| Gene symbol | GCOM1 |
| Synonyms (NCBI Gene) |
GRINL1AGcom2MYZAPMYZAP-POLR2Mgcom
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| Chromosome | 15 |
| Chromosome location | 15q21.3 |
| Summary | This locus represents naturally occurring readthrough transcription between the neighboring MYZAP (myocardial zonula adherens protein) and POLR2M (polymerase (RNA) II (DNA directed) polypeptide M) genes on chromosome 15. Alternative splicing results in mu |
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miRNA
miRNA information provided by mirtarbase database.
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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.).
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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 GCOM1 across shared curated disease and pathway associations.
5
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to GCOM1 (see Related Genes above), that are NOT already directly curated for GCOM1 itself -- a lead worth checking, not a confirmed association.
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