Gene: MOBP

Alternate names for this Gene: -

Gene Summary:

Gene is located in Chromosome: 3

Location in Chromosome : 3p22.1

Description of this Gene: myelin associated oligodendrocyte basic protein

Type of Gene: protein-coding

rs616147 in MOBP gene and AMYOTROPHIC LATERAL SCLEROSIS 1 PMID 28931804 2017 Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.

rs616147 in MOBP gene and AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE PMID 28931804 2017 Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.

rs616147 in MOBP gene and AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder) PMID 28931804 2017 Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.

rs538867 in MOBP gene and Alzheimer's Disease PMID 23535033 2014 Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.

rs616147 in MOBP gene and Amyotrophic Lateral Sclerosis PMID 27455348 2016 Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.

rs616147 in MOBP gene and Amyotrophic Lateral Sclerosis, Sporadic PMID 28931804 2017 Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.

rs864643 in MOBP gene and Attention deficit hyperactivity disorder PMID 18839057 2008 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.

rs1768208 in MOBP gene and Corticobasal degeneration PMID 26077951 2015 Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.

rs1707957 in MOBP gene and Non-obstructive azoospermia PMID 22197933 2011 A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.

rs10675541 in MOBP gene and Progressive supranuclear palsy PMID 30089514 2018 Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases.

PMID 21685912 2011 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.