OMG - oligodendrocyte myelin glycoprotein Gene

Also Known as OMGP

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 4974

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. 상품명 Accession Purity
HY-P75948 OMGP Protein, Human (HEK293, His) P23515-1 (I25-P416) ≥ 95%, as determined by reducing SDS-PAGE.

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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (4)
Cat. No. 상품명
효과
Purity
Rare Diseases
HY-N6669 Methyl 3-O-methylgallate 99.73% Unkown
HY-RS09783 OMG Human Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS17625 Omg Mouse Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS24085 Omg Rat Pre-designed siRNA Set A Pre-designed Set / Unkown

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
Others OMG NCBI