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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

MBP Gene

protein-coding   GIFtS: 67
GCID: GC18M074690

myelin basic protein

 Explore 171 diseases affiliated with
MBP via our new
 Human Malady Compendium 
Biological research products
for MBP
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
Myelin Basic Protein1 2
Myelin A1 Protein2 3
Myelin Membrane Encephalitogenic Protein2 3

External Ids:    HGNC: 69251   Entrez Gene: 41552   Ensembl: ENSG000001979717   OMIM: 1594305   UniProtKB: P026863   

Export aliases for MBP gene to outside databases

Previous GC identifers: GC18M074281 GC18M074839 GC18M074453 GC18M072817 GC18M072819 GC18M071371


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for MBP:
The protein encoded by the classic MBP gene is a major constituent of the myelin sheath of oligodendrocytes and Schwann
cells in the nervous system. However, MBP-related transcripts are also present in the bone marrow and the immune
system. These mRNAs arise from the long MBP gene (otherwise called 'Golli-MBP') that contains 3 additional exons
located upstream of the classic MBP exons. Alternative splicing from the Golli and the MBP transcription start sites
gives rise to 2 sets of MBP-related transcripts and gene products. The Golli mRNAs contain 3 exons unique to
Golli-MBP, spliced in-frame to 1 or more MBP exons. They encode hybrid proteins that have N-terminal Golli aa sequence
linked to MBP aa sequence. The second family of transcripts contain only MBP exons and produce the well characterized
myelin basic proteins. This complex gene structure is conserved among species suggesting that the MBP transcription
unit is an integral part of the Golli transcription unit and that this arrangement is important for the function
and/or regulation of these genes. (provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: MBP_HUMAN, P02686
Function: The classic group of MBP isoforms (isoform 4-isoform 14) are with PLP the most abundant protein components of
the myelin membrane in the CNS. They have a role in both its formation and stabilization. The smaller isoforms might
have an important role in remyelination of denuded axons in multiple sclerosis. The non-classic group of MBP isoforms
(isoform 1-isoform 3/Golli-MBPs) may preferentially have a role in the early developing brain long before myelination,
maybe as components of transcriptional complexes, and may also be involved in signaling pathways in T-cells and neural
cells. Differential splicing events combined with optional post-translational modifications give a wide spectrum of
isomers, with each of them potentially having a specialized function. Induces T-cell proliferation

Gene Wiki entry for MBP (Myelin basic protein)


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000018.9  NC_018929.1  NT_025028.14  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the MBP gene promoter:
         PPAR-alpha   AP-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 2): MBP promoter sequence
   Search SABiosciences Chromatin IP Primers for MBP

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat MBP


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 18q23   Ensembl cytogenetic band:  18q23   HGNC cytogenetic band: 18q23

MBP Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
MBP gene location

GeneLoc information about chromosome 18         GeneLoc Exon Structure

GeneLoc location for GC18M074690:  view genomic region     (about GC identifiers)

Start:
74,690,783 bp from pter      End:
74,845,639 bp from pter
Size:
154,857 bases      Orientation:
minus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: MBP_HUMAN, P02686 (See protein sequence)
Recommended Name: Myelin basic protein  
Size: 304 amino acids; 33117 Da
Subunit: Homodimer. Isoform 3 exists as a homodimer
Subcellular location: Myelin membrane; Peripheral membrane protein; Cytoplasmic side. Note=Cytoplasmic side of myelin
Developmental stage: Expression begins abruptly in 14-16 week old fetuses. Even smaller isoforms seem to be produced
during embryogenesis; some of these persisting in the adult. Isoform 4 expression is more evident at 16 weeks and its
relative proportion declines thereafter
Sequence caution: Sequence=AAC41944.1; Type=Miscellaneous discrepancy; Note=Contaminating sequence. The C-terminus
contains a Histidine tag; Sequence=BAD92223.1; Type=Erroneous initiation; Note=Translation N-terminally shortened;
Sequence=CAH10359.1; Type=Miscellaneous discrepancy; Note=wrong intron-exon boundaries;
6 PDB 3D structures from and Proteopedia for MBP:
1BX2 (3D)        1FV1 (3D)        1HQR (3D)        1QCL (3D)        1YMM (3D)        1ZGL (3D)    
Secondary accessions: A4FU54 A6NI84 A8MY86 A8MYL4 B3KY66 B7ZKS2 B7ZKS4 Q15337 Q15338 Q15339 Q15340
Q59GX3 Q65ZS4 Q6AI64 Q6FH37 Q6FI04 Q6PK23
Alternative splicing: 6 isoforms:  P02686-1   P02686-2   P02686-3   P02686-4   P02686-5   P02686-6   (Initiator Met-1 is removed. Contains a N-acetylalanine at position 2)

Explore the universe of human proteins at neXtProt for MBP: NX_P02686

Post-translational modifications:

  • Several charge isomers of MBP; C1 (the most cationic, least modified, and most abundant form), C2, C3, C4, C5, C6, C7,
  • C8-A and C8-B (the least cationic form); are produced as a result of optional PTM, such as phosphorylation,
    deamidation of glutamine or asparagine, arginine citrullination and methylation. C8-A and C8-B contain each two mass
    isoforms termed C8-A(H), C8-A(L), C8-B(H) and C8-B(L), (H) standing for higher and (L) for lower molecular weight. C3,
    C4 and C5 are phosphorylated. The ratio of methylated arginine residues decreases during aging, making the protein
    more cationic1
  • The N-terminal alanine is acetylated (isoform 3, isoform 4, isoform 5 and isoform 6)1
  • Arg-241 was found to be 6% monomethylated and 60% symmetrically dimethylated1
  • Phosphorylated by TAOK2, VRK2, MAPK11, MAPK12, MAPK14 and MINK11
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P02686

  • MBP Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (6 alternative transcripts): 
    NP_001020252.1  NP_001020261.1  NP_001020263.1  NP_001020271.1  NP_001020272.1  NP_002376.1  

    ENSEMBL proteins: 
     ENSP00000372025   ENSP00000462734   ENSP00000380973   ENSP00000380964   ENSP00000380963  
     ENSP00000435243   ENSP00000352667   ENSP00000436830   ENSP00000462780   ENSP00000431267  
     ENSP00000380967   ENSP00000346545   ENSP00000431335   ENSP00000462758   ENSP00000434011  
     ENSP00000435641   ENSP00000462223   ENSP00000463780   ENSP00000463403   ENSP00000405882  
     ENSP00000432988   ENSP00000442393   ENSP00000436951   ENSP00000463137   ENSP00000435322  
     ENSP00000437063   ENSP00000380961   ENSP00000380958   ENSP00000462374   ENSP00000463164  
     ENSP00000348273  

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    Uscn Proteins for MBP

    Gene Ontology (GO): 5/6 cellular component terms (GO ID links to tree view) (see all 6):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005886plasma membrane IEA--
    GO:0033269internode region of axon IEA--
    GO:0042995cell projection ----
    GO:0043025neuronal cell body IEA--
    GO:0043209myelin sheath ----


    MBP for ontologies           About GeneDecksing



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    Uscn ELISAs and CLIAs for MBP


    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    MBP for domains           About GeneDecksing

    1 InterPro domain/family:
     IPR000548 Myelin_BP

    Graphical View of Domain Structure for InterPro Entry P02686

    ProtoNet protein and cluster: P02686

    1 Blocks protein family: IPB000548 Myelin basic protein

    UniProtKB/Swiss-Prot: MBP_HUMAN, P02686
    Similarity: Belongs to the myelin basic protein family


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Function Summary:

         UniProtKB/Swiss-Prot: MBP_HUMAN, P02686
    Function: The classic group of MBP isoforms (isoform 4-isoform 14) are with PLP the most abundant protein components of
    the myelin membrane in the CNS. They have a role in both its formation and stabilization. The smaller isoforms might
    have an important role in remyelination of denuded axons in multiple sclerosis. The non-classic group of MBP isoforms
    (isoform 1-isoform 3/Golli-MBPs) may preferentially have a role in the early developing brain long before myelination,
    maybe as components of transcriptional complexes, and may also be involved in signaling pathways in T-cells and neural
    cells. Differential splicing events combined with optional post-translational modifications give a wide spectrum of
    isomers, with each of them potentially having a specialized function. Induces T-cell proliferation

         Genatlas biochemistry entry for MBP:
    myelin,basic protein,major component of normal myelin of central nervous system,with three alternatively spliced
    isoforms

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    hsa-miR-2052 hsa-miR-34b* hsa-miR-16-2* hsa-miR-1258 hsa-miR-3653 hsa-miR-132 hsa-miR-449a hsa-miR-1323
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    Gene Ontology (GO): 2 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0002020protease binding IEA--
    GO:0019911structural constituent of myelin sheath IEA--


    MBP for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for MBP:
     Increased gamma-H2AX phosphory 

    Animal Models:
         Mouse knock-out Mbptm1Atc for MBP
         11 MGI mutant phenotypes (inferred from 5 alleles(MGI details for Mbp):
     behavior/neurological  cellular  hearing/vestibular/ear  hematopoietic system  homeostasis/metabolism 
     immune system  mortality/aging  nervous system  normal  reproductive system 
     vision/eye 

    MBP for phenotypes           About GeneDecksing


    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
    About This Section

    Unified GeneCards pathways  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Selected targets of C/EBPbeta
    Selected targets of C/EBPbeta1.00
    2Glial Cell Differentiation
    Glial Cell Differentiation1.00
    3Neural Crest Differentiation
    Neural Crest Differentiation1.00
    4G-protein signaling_Ras family GTPases in kinase cascades (scheme)
    MAPK Cascade0.44
    5Cell adhesion_ECM remodeling
    Metalloproteases in connective tissue degradation0.31

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    2 EMD Millipore Pathways for MBP
        Selected targets of C/EBPbeta
    Metalloproteases in connective tissue degradation


    3 BioSystems Pathways for MBP 
        Neural Crest Differentiation
    MAPK Cascade
    Glial Cell Differentiation



    MBP for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for MBP

    STRING Interaction Network Preview (showing 5 interactants - click image to see 25)

    5/74 Interacting proteins for MBP (P026862, 3 ENSP000003482734) via UniProtKB, MINT, STRING, and/or I2D (see all 74)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    APTXQ7Z2E32, 3, ENSP000004008064MINT-2860724 I2D: score=3 STRING: ENSP00000400806
    ATN1P542592, 3, ENSP000003490764MINT-2860743 I2D: score=3 STRING: ENSP00000349076
    MAPK1P284822, 3, ENSP000002158324MINT-4301912 I2D: score=1 STRING: ENSP00000215832
    CALM1P621583I2D: score=1 
    CALM2P621583I2D: score=1 
    About this table

    Gene Ontology (GO): 5/8 biological process terms (GO ID links to tree view) (see all 8):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006955immune response TAS7504278
    GO:0007268synaptic transmission TAS2434243
    GO:0007417central nervous system development TAS2434243
    GO:0008366axon ensheathment TAS2434243
    GO:0009636response to toxin IEA--


    MBP for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section

    MBP for compounds           About GeneDecksing

    Browse Small Molecules at EMD Millipore
    Enzo Life Sciences drugs & compounds for MBP

    Compounds for MBP available from Tocris Bioscience    About this table
    CompoundAction CAS #
    Myelin Basic Protein (87-99)Major antigenic component implicated in the pathophysiology of multiple sclerosis[118506-26-6]

    1 HMDB Compound for MBP    About this table
    CompoundSynonyms CAS #PubMed Ids
    3-O-Sulfogalactosylceramide (d18:1/24:0)Sulfatide (d18:1/24:0) (see all 16)151122-71-32480186
    10/101 Novoseek chemical compound relationships for MBP gene (see all 101)    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    2',3'-cyclic nucleotide 87.3 59 11279272 (2), 11356257 (2), 1964183 (1), 8416742 (1) (see all 39)
    glatiramer acetate 78.9 106 9237101 (7), 7541725 (5), 10861011 (4), 8965119 (3) (see all 28)
    copolymer i 69.6 9 1707304 (3), 1714060 (1), 11003134 (1)
    cuprizone 62.8 5 18938062 (1), 20305752 (1), 17290413 (1)
    threonine 59.4 24 1315774 (1), 14594813 (1), 1716348 (1), 1716457 (1) (see all 20)
    benzophenone-3 55.6 9 7679413 (1), 16049372 (1), 7517457 (1), 11207660 (1) (see all 7)
    sulfatide 55.4 22 18039685 (3), 9482258 (2), 1372178 (2), 12161033 (1) (see all 10)
    sulf 54.4 12 9130259 (4), 1372178 (3), 12161033 (1)
    citrulline 53.2 36 1707596 (2), 7683860 (2), 7507225 (2), 10675299 (2) (see all 15)
    edss 50.1 3 9619641 (1), 9987755 (1)

    Search CenterWatch for drugs/clinical trials and news about MBP 

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
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    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for MBP gene (8 alternative transcripts): 
    NM_001025081.1  NM_001025090.1  NM_001025092.1  NM_001025100.1  NM_001025101.1  NM_002385.2  NM_001025094.1  NM_001025098.1  

    Unigene Cluster for MBP:

    Myelin basic protein
    Hs.551713  [show with all ESTs]
    Unigene Representative Sequence: NM_001025100
    18/48 Ensembl transcripts including schematic representations, and UCSC links where relevant (see all 48):
    ENST00000382582 ENST00000490319(uc010dqz.3) ENST00000585201(uc010xfe.1)
    ENST00000397875 ENST00000397866 ENST00000397865 ENST00000527041 ENST00000359645
    ENST00000528160 ENST00000577755 ENST00000527975 ENST00000578715 ENST00000397869
    ENST00000354542 ENST00000531144 ENST00000583474 ENST00000533278 ENST00000526111


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    Additional cDNA sequence: 

    AB208986.1 AK074315.1 AK093588.1 AK094611.1 AK095121.1 AK098402.1 AK098513.1 AK122594.1 
    AK123433.1 AK124830.1 AK126977.1 AK128770.1 AK128788.1 AK289893.1 AK293922.1 AK296492.1 
    AK314553.1 BC008749.2 BC030093.1 BC065248.1 BC068550.1 BC080654.1 BC101771.1 BC101773.1 
    BC130034.1 BC143348.1 BC143350.1 CR536534.1 CR541919.1 L18865.1 M13577.1 M30047.1 
    M30515.1 M30516.1 

    24/159 DOTS entries (see all 159):

    DT.100889742  DT.101985667  DT.95223942  DT.95095286  DT.91848616  DT.95095349  DT.121101020  DT.121100766 
    DT.95310721  DT.100889773  DT.121100675  DT.100889749  DT.95211483  DT.121101087  DT.100889740  DT.91873487 
    DT.86855495  DT.121100576  DT.95164195  DT.100889757  DT.111002  DT.100889751  DT.100889768  DT.121100982 

    24/1185 AceView cDNA sequences (see all 1185):

    BF727350 CB155773 BP349448 AV729124 CK431001 CF453545 AA348363 AL533010 
    AA321160 AA348829 CB153591 F06160 AA889895 AA348803 BM977303 BP360101 
    BQ893737 AA348606 CB155578 CB155812 AI580896 CB152243 AI128878 BI039212 

    GeneLoc Exon Structure

    5/15 Alternative Splicing Database (ASD) splice patterns (SP) for MBP (see all 15)    About this scheme

    ExUns: 1 ^ 2 ^ 3 ^ 4a · 4b ^ 5 ^ 6a · 6b ^ 7a · 7b · 7c · 7d · 7e ^ 8 ^ 9 ^ 10a · 10b · 10c ^ 11 ^ 12a · 12b ^ 13a · 13b · 13c ^ 14a · 14b ·
    SP1:                                                                          -           -                 -                 -     -                           
    SP2:                                                                          -     -     -                 -                 -     -                           
    SP3:                                                                          -           -                 -           -     -     -                           
    SP4:                                                                          -     -     -                 -           -     -     -                           
    SP5:                                                                    -     -     -     -     -     -     -     -     -     -     -     -                     

    ExUns: 14c · 14d ^ 15a · 15b
    SP1:                        
    SP2:                        
    SP3:                        
    SP4:                        
    SP5:                        


    ECgene alternative splicing isoforms for MBP

    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    MBP expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: TCTATTAATA

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)

    About this image

    MBP expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    7 LifeMap In Vivo Development Anatomical Compartments/Cells 
    Tissue Anatomical Compartment CellCategory (developmental path)
    OvaryAntral FollicleCumulus CellsOvary
    Spinal CordSpinal Ventral ColumnsVentral Spinal Cord Progenitor CellsMotor Neurons
    BoneZeugopod Growth PlateBone
    BoneZeugopod PeriosteumBone
    BrainMedulla OblongataBrain
    KidneyRenal Collecting Duct SystemKidney
    Spinal CordSpinal Ventral ColumnsSpinal Cord
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization
    Stem Cell Differentiation: 1 LifeMap Cell 
    NameCategory
    PureStem™ progenitor Z1 (Embryonic Progenitor Cell)

    See MBP Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for MBP

    SOURCE GeneReport for Unigene cluster: Hs.551713

    UniProtKB/Swiss-Prot: MBP_HUMAN, P02686
    Tissue specificity: MBP isoforms are found in both the central and the peripheral nervous system, whereas Golli-MBP
    isoforms are expressed in fetal thymus, spleen and spinal cord, as well as in cell lines derived from the immune
    system

        SABiosciences Expression via Pathway-Focused PCR Arrays including MBP: 
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              Multiple Sclerosis in human mouse rat

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    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of chordates.

    Orthologs for MBP gene from 5/9 species (see all 9)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Mbp1 , 5 myelin basic protein1, 5 88.35(n)1
    87.55(a)1
      18 (55.84 cM)5
    171961  NM_010777.31  NP_034907.11 
     824751465 
    chicken
    (Gallus gallus)
    Aves MBP1 myelin basic protein 71.86(n)
    73.65(a)
      396217  NM_205280.1  NP_990611.1 
    lizard
    (Anolis carolinensis)
    Reptilia MBP6
    --
    43(a)
    1 ↔ 1
    4(50865105-50900400)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.257242 Xenopus laevis mRNA for myelin basic protein, complete more 77.52(n)    AB000736.1 
    zebrafish
    (Danio rerio)
    Actinopterygii mbpb1 myelin basic protein b 60.88(n)
    55.37(a)
      368319  XM_001923576.2  XP_001923611.1 


    ENSEMBL Gene Tree for MBP (if available)
    TreeFam Gene Tree for MBP (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
      --

    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    10/3481 NCBI SNPs in MBP are shown (see all 3481    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 18 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs4703191,2
    C,F,A,--74690322(+) TAAGAT/GCCTGT 5 -- ds50018Minor allele frequency- G:0.21NA WA EA 368
    rs1420049731,2
    C,--74690349(+) AAAAC-/AAAAGAG 5 -- ds50010--------
    rs1868538441,2
    --74690349(+) AAAACA/GAAAGA 5 -- ds50010--------
    rs1448875941,2
    --74690357(+) AGAGAA/CTTTCG 5 -- ds50010--------
    rs1131698211,2
    C,--74690361(+) ACTTTC/TGTCTA 5 -- ds50012Minor allele frequency- T:0.05CSA WA 120
    rs1886015651,2
    --74690556(+) GAGACA/GCTAAA 5 -- ds50010--------
    rs65659231,2
    C,F,A,H,--74690596(+) CCTAAC/AAACTA 5 -- ds500111Minor allele frequency- A:0.07NS EA NA WA 922
    rs99652581,2
    C,--74690680(+) GCCCTG/ACCTGG 5 -- ds50012Minor allele frequency- A:0.06CSA WA 120
    rs22762761,2
    C,F,A,--74690684(+) TGCCTG/CGAGAC 5 -- ds500114Minor allele frequency- C:0.32NA EA WA CSA 732
    rs22762771,2
    C,F,H,--74690700(+) GGCACC/TGAGTC 5 -- ds500132Minor allele frequency- T:0.30NA NS EA WA 3268

    HapMap Linkage Disequilibrium report for MBP (74690783 - 74845639 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 6 variations for MBP
         1 CNV: 102725
         5 Indels: 45692 61643 26116 42949 102726

    SABiosciences Cancer Mutation PCR Assays
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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    MBP for disorders           About GeneDecksing

    OMIM gene information: 159430    OMIM disorders: --

    UniProtKB/Swiss-Prot: MBP_HUMAN, P02686
  • Note=The reduction in the surface charge of citrullinated and/or methylated MBP could result in a weakened
  • attachment to the myelin membrane. This mechanism could be operative in demyelinating diseases such as chronical
    multiple sclerosis (MS), and fulminating MS (Marburg disease)

    20/171 diseases for MBP (see all 171):    About MalaCards
    htlv-1 associated myelopathy/tropical spastic paraparesis    htlv-1 associated myelopathy    pelizaeus-merzbacher disease    akinetic mutism
    guillain-barre syndrome    landau-kleffner syndrome    central pontine myelinolysis    tropical spastic paraparesis
    neuromyelitis optica    spinal cord injury    malignant peripheral nerve sheath tumor    relapsing-remitting multiple sclerosis
    chiari malformation    chronic inflammatory demyelinating polyradiculoneuropathy    transverse myelitis    niemann-pick disease
    aids dementia complex    ossifying fibromyxoid tumor    acid sphingomyelinase deficiency    subacute sclerosing panencephalitis

    8 diseases from the University of Copenhagen DISEASES database for MBP:
    Multiple sclerosis     Acute disseminated encephalomyelitis     Hypersensitivity reaction type II disease     Brain disease
    Neuropathy     Measles     Neuromyelitis optica     Subacute sclerosing panencephalitis

    10/96 Novoseek disease relationships for MBP gene (see all 96)    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    multiple sclerosis 92.5 562 14714495 (7), 1690527 (4), 12465458 (4), 1694970 (4) (see all 99)
    encephalomyelitis 89.8 187 7512579 (2), 7689596 (2), 7504090 (2), 15292513 (2) (see all 99)
    demyelinating diseases 86.7 49 1384994 (2), 1718484 (1), 8632058 (1), 11234279 (1) (see all 30)
    demyelination 85.6 88 19726693 (2), 7508580 (2), 12465458 (2), 7525334 (2) (see all 60)
    18q- syndrome 74.4 5 8507907 (1), 9259379 (1), 8767586 (1), 14508777 (1)
    autoimmune diseases 72.7 29 8393796 (1), 10377791 (1), 8590314 (1), 7692995 (1) (see all 20)
    encephalomyelitis acute disseminated 70.6 2 12589368 (1), 17990580 (1)
    optic neuritis 70.4 16 7510787 (2), 7515411 (2), 7513391 (1), 7524258 (1) (see all 10)
    autoimmune response 69.8 29 1718484 (1), 7689820 (1), 7526591 (1), 9394837 (1) (see all 16)
    myelin degeneration 63.6 5 20091409 (1), 9094982 (1), 16900293 (1), 19359623 (1) (see all 5)

    Genetic Association Database (GAD): MBP
    Human Genome Epidemiology (HuGE) Navigator: MBP (391 documents)

    Export disorders for MBP gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

    PubMed articles for MBP gene, integrated from 9 sources (see all 1256):
    (articles sorted by number of sources associating them with MBP)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Identification of three forms of human myelin basic protein by cDNA cloning. (PubMed id 2425357)1, 2, 3 Kamholz J.... Lazzarini R.A. (1986)
    2. [Polymorphism of length of tetranucleotide repeat from the 5'-side from the myelin basic protein gene in multiple sclerosis in Russians] (PubMed id 14714495)1, 4, 9 Andreevskii T.V....Favorova O.O. (2003)
    3. Myelin basic protein gene is associated with MS in DR4- and DR5-positive Italians and Russians. (PubMed id 12939427)1, 4, 9 Guerini F.R....Favorova O.O. (2003)
    4. The isolation and characterization of four myelin basic proteins from the unbound fraction during CM52 chromatography. (PubMed id 7574672)1, 2, 9 Boulias C.... Moscarello M.A. (1995)
    5. Leukocyte gelatinase B cleavage releases encephalitogens from human myelin basic protein. (PubMed id 7685161)1, 2, 9 Proost P.... Opdenakker G. (1993)
    6. Structure of a human autoimmune TCR bound to a myelin basic protein self-peptide and a multiple sclerosis-associated MHC class II molecule. (PubMed id 16079912)1, 2 Li Y.... Mariuzza R.A. (2005)
    7. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
    8. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    9. Genetic variation of mannose-binding protein associated with glomerular immune deposition in IgA nephropathy. (PubMed id 11940329)1, 4 Gong R....Li L. (2002)
    10. [Mannose-binding protein gene polymorphism influences the patterns of glomerular immune deposition in IgA nephropathy] (PubMed id 11295122)1, 4 Gong R....Li L. (2001)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 4155 HGNC: 6925 AceView: MBP Ensembl:ENSG00000197971 euGenes: HUgn4155
    ECgene: MBP H-InvDB: MBP

    (According to HUGE)
    About This Section
      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for MBP Pharmacogenomics, SNPs, Pathways
    Wikipedia http://en.wikipedia.org/wiki/Myelin_basic_protein

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for MBP gene:
    Search GeneIP for patents involving MBP

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



    (Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences),
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    About This Section

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