OPALIN (oligodendrocytic myelin paranodal and inner loop protein)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 93377 |
| Gene name | Oligodendrocytic myelin paranodal and inner loop protein |
| Gene symbol | OPALIN |
| Synonyms (NCBI Gene) |
HTMP10TMEM10TMP10
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| Chromosome | 10 |
| Chromosome location | 10q24.1 |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q96PE5 | |
| Protein name | Opalin (Oligodendrocytic myelin paranodal and inner loop protein) (Transmembrane protein 10) | |
| Protein function | Central nervous system-specific myelin protein that increase myelin genes expression during oligodendrocyte differentiation. Promotes oligodendrocyte terminal differentiation. | |
| Family and domains | ||
| Tissue specificity | TISSUE SPECIFICITY: Brain specific; expressed in oligodendrocytes (PubMed:11814680, PubMed:30837646). Expressed in oligodendrocytes in remyelinating multiple sclerosis plaques (PubMed:30837646). {ECO:0000269|PubMed:11814680, ECO:0000269|PubMed:30837646}. | |
| Sequence |
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| Sequence length | 141 | |
| Interactions | View interactions | |
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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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