1. Gene
  2. OMG - oligodendrocyte myelin glycoprotein Gene

OMG - oligodendrocyte myelin glycoprotein Gene

Homo sapiens

Also known as OMGP

Gene ID: 4974 | Gene type: protein coding

About OMG

Cytogenetic location: 17q11.2 Genomic coordinates (GRCh38): 17:31,294,647-31,297,239 (from NCBI)

This gene has 4 transcripts (splice variants), 250 orthologues and 10 paralogues. Restricted expression toward brain (RPKM 57.3).

Summary

Predicted to enable identical protein binding activity. Predicted to be involved in neuron projection regeneration. Predicted to act upstream of or within regulation of collateral sprouting of intact axon in response to injury. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

OMG Products(1)

mRNA Protein Name
NM_002544.5 NP_002535.3 oligodendrocyte-myelin glycoprotein precursor

OMG Protein Structure

LRRNT

LRRNT: Leucine rich repeat N-terminal domain (25 - 54)

LRR_4

LRR_4: Leucine Rich repeats (2 copies) (56 - 95)

LRR_6

LRR_6: Leucine Rich repeat (145 - 158)

LRR_8

LRR_8: Leucine rich repeat (168 - 226)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 440 a.a.
Protein Preferred Names Protein Names

oligodendrocyte-myelin glycoprotein

Recombinant OMG Proteins

Cat. No. Product Name Accession Purity
HY-P75948 OMGP Protein, Human (HEK293, His) P23515-1 (I25-P416) ≥95%

Related Diseases

Diseases Alias
Neurofibromatosis, Type I

Von Recklinghausen Disease

Neurofibromatosis 1

Neurofibromatosis, Type 1

NF1

Neurofibromatosis, Peripheral Type

Neurofibromatosis Type I

Neurofibromatosis Type 1 Due To Nf1 Mutation Or Intragenic Deletion

Familial Spinal Neurofibromatosis

Fsnf

Peripheral Neurofibromatosis

Von Recklinghausen'S Neurofibromatosis

Von Recklinghausen Disease Due To Nf1 Mutation Or Intragenic Deletion

Neurofibromatosis Peripheral Type

Von Recklinghausen Syndrome

Neurofibromatosis Type 1

Von Recklinghausen Neuropathy

Nf1 - [Neurofibromatosis Type 1]

Recklinghausen Disease

Internuclear Ophthalmoplegia

Ophthalmoplegia Internuclearis

Bielschowsky-Lutz-Cogan Syndrome

Ino - [Internuclear Ophthalmoplegia]

Lhermitte Syndrome

Mlf - [Medial Longitudinal Fasciculus] Syndrome

Internuclear Paralysis

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta OMG VGNC VGNC:75584
Mus musculus OMG MGD MGI:106586
Bos taurus OMG VGNC VGNC:50238
Felis catus OMG VGNC VGNC:99315
Rattus norvegicus OMG RGD RGD:1359125
Canis familiaris OMG VGNC VGNC:49934
Susscrofa domestica OMG NCBI
Others OMG NCBI