Gene Gene information from NCBI Gene database.
Entrez ID 93377
Gene name Oligodendrocytic myelin paranodal and inner loop protein
Gene symbol OPALIN
Synonyms (NCBI Gene)
HTMP10TMEM10TMP10
Chromosome 10
Chromosome location 10q24.1
miRNA miRNA information provided by mirtarbase database.
78
miRTarBase ID miRNA Experiments Reference
MIRT645823 hsa-miR-6769a-3p HITS-CLIP 23824327
MIRT645822 hsa-miR-186-3p HITS-CLIP 23824327
MIRT645823 hsa-miR-6769a-3p HITS-CLIP 23824327
MIRT645822 hsa-miR-186-3p HITS-CLIP 23824327
MIRT1204057 hsa-miR-1224-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0005794 Component Golgi apparatus IDA
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane ISS
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617200 20707 ENSG00000197430
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
MSFSLNFTLPANTTSSPVTGGKETDCGPSLGLAAGIPLLVATALLVALLFTLIHRRRSSI
EAMEESDRPCEISEIDDNPKISENPRRSPTHEKNTMGAQEAHIYVKTVAGSEEPVHDRYR
PTIEMERRRGLWWLVPRLSLE
Sequence length 141
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
DEMENTIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Demyelinating Diseases Demyelinating Diseases BEFREE 30837646
★☆☆☆☆
Found in Text Mining only
Focal Cortical Dysplasia Focal cortical dysplasia Pubtator 34301297 Associate
★☆☆☆☆
Found in Text Mining only
Focal cortical dysplasia of Taylor Focal cortical dysplasia Pubtator 34301297 Associate
★☆☆☆☆
Found in Text Mining only
Glioblastoma Glioblastoma Pubtator 34516348 Associate
★☆☆☆☆
Found in Text Mining only
Prostatic Neoplasms Prostatic neoplasm Pubtator 35358005 Associate
★☆☆☆☆
Found in Text Mining only