MBP, myelin basic protein, 4155

N. diseases: 184; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2000811
rs2000811
Entrez Id: 4155
Gene Symbol: MBP
MBP
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.710 GeneticVariation GWASDB Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis--a genome-wide study combined with immunological analyses. 21673997 2011
dbSNP: rs2000811
rs2000811
Entrez Id: 4155
Gene Symbol: MBP
MBP
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.710 GeneticVariation BEFREE A novel risk variant, rs2000811, in intron2 of the myelin basic protein (MBP) at chromosome 18q23 showed strong association with RA (p = 2.7×10(-8), OR 1.23, 95% CI: 1.14-1.32). 21673997 2011
dbSNP: rs12458282
rs12458282
Entrez Id: 4155
Gene Symbol: MBP
MBP
CUI: C0038436
Disease:
Post-Traumatic Stress Disorder
0.010 GeneticVariation BEFREE We found that there is a possibility for a correlation of the T allele rs12458282 within the MBP gene with higher CAPS scores in lifetime PTSD patients which would need to be tested in a sample providing more statistical power. 31291231 2019
dbSNP: rs1026520
rs1026520
Entrez Id: 4155
Gene Symbol: MBP
MBP
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE Coincidentally, the haplotype containing the rs1026520-C and rs9794-C alleles was also associated with a statistically decreased risk of abdominal obesity after covariate adjustment (OR = 0.59, 95% CI = 0.45-0.77, p < 0.001). 26073637 2016
dbSNP: rs8094402
rs8094402
Entrez Id: 4155
Gene Symbol: MBP
MBP
CUI: C0079744
Disease:
Diffuse Large B-Cell Lymphoma
0.010 GeneticVariation BEFREE A SNP-based analysis showed that MBP rs8094402 was associated with decreased risks of overall NHL (allele risk OR = 0.72, P-trend = 0.0018), DLBCL (allele risk OR = 0.72, P-trend = 0.036), and FL (allele risk OR = 0.67, P-trend = 0.021), while MASP2 rs12711521 was associated with a decreased risk of DLBCL (allele risk OR = 0.57, P-trend = 0.0042). 23055202 2013
dbSNP: rs8094402
rs8094402
Entrez Id: 4155
Gene Symbol: MBP
MBP
CUI: C0024305
Disease:
Lymphoma, Non-Hodgkin
0.010 GeneticVariation BEFREE A SNP-based analysis showed that MBP rs8094402 was associated with decreased risks of overall NHL (allele risk OR = 0.72, P-trend = 0.0018), DLBCL (allele risk OR = 0.72, P-trend = 0.036), and FL (allele risk OR = 0.67, P-trend = 0.021), while MASP2 rs12711521 was associated with a decreased risk of DLBCL (allele risk OR = 0.57, P-trend = 0.0042). 23055202 2013
dbSNP: rs8094402
rs8094402
Entrez Id: 4155
Gene Symbol: MBP
MBP
CUI: C0024301
Disease:
Lymphoma, Follicular
0.010 GeneticVariation BEFREE A SNP-based analysis showed that MBP rs8094402 was associated with decreased risks of overall NHL (allele risk OR = 0.72, P-trend = 0.0018), DLBCL (allele risk OR = 0.72, P-trend = 0.036), and FL (allele risk OR = 0.67, P-trend = 0.021), while MASP2 rs12711521 was associated with a decreased risk of DLBCL (allele risk OR = 0.57, P-trend = 0.0042). 23055202 2013
dbSNP: rs3794845
rs3794845
Entrez Id: 4155
Gene Symbol: MBP
MBP
CUI: C0023449
Disease:
Acute lymphocytic leukemia
0.010 GeneticVariation BEFREE Subgroup analysis showed that Ly96 rs78380171 and MBP rs3794845 were significantly associated with the risk of acute lymphoblastic leukemia (p(trend) < 0.001). 20438785 2010
dbSNP: rs3794845
rs3794845
Entrez Id: 4155
Gene Symbol: MBP
MBP
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma
0.010 GeneticVariation BEFREE Subgroup analysis showed that Ly96 rs78380171 and MBP rs3794845 were significantly associated with the risk of acute lymphoblastic leukemia (p(trend) < 0.001). 20438785 2010
dbSNP: rs3794845
rs3794845
Entrez Id: 4155
Gene Symbol: MBP
MBP
CUI: C1332977
Disease:
Childhood Leukemia
0.010 GeneticVariation BEFREE Three SNPs (STAT6 rs703817, C1qG rs17433222, and MBP rs3794845) were significantly associated with childhood leukemia risk (p(trend) < 0.001, minP < 0.01). 20438785 2010
dbSNP: rs1337832380
rs1337832380
Entrez Id: 4155
Gene Symbol: MBP
MBP
CUI: C1611743
Disease:
Familial (FPAH)
0.010 GeneticVariation BEFREE Our previous studies determined that myelin basic protein (MBP) was capable of inhibiting fibril formation of a highly fibrillogenic Abeta peptide containing both E22Q (Dutch) and D23N (Iowa) mutations associated with familial forms of cerebral amyloid angiopathy [Hoos, M. D., et al.(2007) J. Biol.Chem.282, 9952-9961]. 19385666 2009
dbSNP: rs1337832380
rs1337832380
Entrez Id: 4155
Gene Symbol: MBP
MBP
CUI: C0085220
Disease:
Cerebral Amyloid Angiopathy
0.010 GeneticVariation BEFREE Our previous studies determined that myelin basic protein (MBP) was capable of inhibiting fibril formation of a highly fibrillogenic Abeta peptide containing both E22Q (Dutch) and D23N (Iowa) mutations associated with familial forms of cerebral amyloid angiopathy [Hoos, M. D., et al.(2007) J. Biol.Chem.282, 9952-9961]. 19385666 2009
dbSNP: rs1194494874
rs1194494874
Entrez Id: 4155
Gene Symbol: MBP
MBP
CUI: C0014070
Disease:
Encephalomyelitis
0.010 GeneticVariation BEFREE We found that mMOG-35-55 peptide was strongly immunogenic and induced moderately severe chronic experimental autoimmune encephalomyelitis (EAE) with white matter lesions after a single injection in Freund's complete adjuvant followed by pertussis toxin. hMOG-35-55 peptide,which differs from mMOG-35-55 peptide by a proline for serine substitution at position 42, was also immunogenic, but not encephalitogenic, and was only partially cross-reactive with mMOG-35-55. 15114658 2004