Gene Gene information from NCBI Gene database.
Entrez ID 4974
Gene name Oligodendrocyte myelin glycoprotein
Gene symbol OMG
Synonyms (NCBI Gene)
OMGP
Chromosome 17
Chromosome location 17q11.2
miRNA miRNA information provided by mirtarbase database.
8
miRTarBase ID miRNA Experiments Reference
MIRT1551930 hsa-miR-208a CLIP-seq
MIRT1551931 hsa-miR-208b CLIP-seq
MIRT1551932 hsa-miR-3617 CLIP-seq
MIRT1551933 hsa-miR-3658 CLIP-seq
MIRT1551934 hsa-miR-499-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane TAS
GO:0007155 Process Cell adhesion IEA
GO:0016020 Component Membrane IEA
GO:0031102 Process Neuron projection regeneration IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
164345 8135 ENSG00000126861
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P23515
Protein name Oligodendrocyte-myelin glycoprotein
Protein function Cell adhesion molecule contributing to the interactive process required for myelination in the central nervous system.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01462 LRRNT 25 54 Leucine rich repeat N-terminal domain Family
PF00560 LRR_1 79 102 Leucine Rich Repeat Repeat
PF13855 LRR_8 167 226 Leucine rich repeat Repeat
Tissue specificity TISSUE SPECIFICITY: Oligodendrocytes and myelin of the central nervous system.
Sequence
MEYQILKMSLCLFILLFLTPGILCICPLQCICTERHRHVDCSGRNLSTLPSGLQENIIHL
NLSYNHFTDLHNQLTQYTNLRTLDISNNRLESLPAHLPRSLWNMSAANNNIKLLDKSDTA
YQWNLKYLDVSKNMLEKVVLIKNTLRSLEVLNLSSNKLWTVPTNMPSKLHIVDLSNNSLT
QILPGTLINLTNLTHLYLHNNKFTFIPDQSFDQLFQLQEITLYNNR
WSCDHKQNITYLLK
WMMETKAHVIGTPCSTQISSLKEHNMYPTPSGFTSSLFTVSGMQTVDTINSLSVVTQPKV
TKIPKQYRTKETTFGATLSKDTTFTSTDKAFVPYPEDTSTETINSHEAAAATLTIHLQDG
MVTNTSLTSSTKSSPTPMTLSITSGMPNNFSEMPQQSTTLNLWREETTTNVKTPLPSVAN
AWKVNASFLLLLNVVVMLAV
Sequence length 440
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Axonal growth inhibition (RHOA activation)
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
DIVERTICULAR DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OMG-related disorder Likely benign; Benign ClinVar
★★☆☆☆
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
Autistic Disorder Autism BEFREE 12566166
★☆☆☆☆
Found in Text Mining only
Blepharoptosis Ptosis BEFREE 31734908, 31847046
★☆☆☆☆
Found in Text Mining only
Brain Neoplasms Brain Neoplasms BEFREE 30206994
★☆☆☆☆
Found in Text Mining only
Cerebrovascular accident Stroke BEFREE 16782355
★☆☆☆☆
Found in Text Mining only
Demyelinating Diseases Demyelinating Diseases BEFREE 27933584
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus, Non-Insulin-Dependent Diabetes Mellitus BEFREE 27761984
★☆☆☆☆
Found in Text Mining only
Epilepsy Partial with Variable Foci Progressive myoclonic epilepsy Pubtator 27874947 Associate
★☆☆☆☆
Found in Text Mining only
Glut1 Deficiency Syndrome GLUT1 Deficiency Syndrome BEFREE 20630673
★☆☆☆☆
Found in Text Mining only
Intellectual Disability Mental retardation BEFREE 16425041
★☆☆☆☆
Found in Text Mining only
Intellectual Disability Mental retardation LHGDN 16425041
★☆☆☆☆
Found in Text Mining only