Homo sapiens myelin associated oligodendrocyte basic protein (MOBP), t - Nucleotide

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MOBP rs616147 Polymorphism and Risk of Amyotrophic Lateral Sclerosis in a Greek Population: A Case-Control Study. [Medicina (Kaunas). 2021]
MOBP rs616147 Polymorphism and Risk of Amyotrophic Lateral Sclerosis in a Greek Population: A Case-Control Study.
Liampas I, Siokas V, Aloizou AM, Bakirtzis C, Tsouris Z, Nousia A, Nasios G, Papadimitriou D, Liakos P, Bogdanos DP, et al. Medicina (Kaunas). 2021 Dec 7; 57(12). Epub 2021 Dec 7.
Myelin-associated oligodendrocyte basic protein rs616147 polymorphism as a risk factor for Parkinson's disease. [Acta Neurol Scand. 2022]
Myelin-associated oligodendrocyte basic protein rs616147 polymorphism as a risk factor for Parkinson's disease.
Siokas V, Aloizou AM, Liampas I, Bakirtzis C, Tsouris Z, Sgantzos M, Liakos P, Bogdanos DP, Hadjigeorgiou GM, Dardiotis E. Acta Neurol Scand. 2022 Feb; 145(2):223-228. Epub 2021 Oct 25.
MOBP and HIP1 in multiple system atrophy: New α-synuclein partners in glial cytoplasmic inclusions implicated in the disease pathogenesis. [Neuropathol Appl Neurobiol. 2021]
MOBP and HIP1 in multiple system atrophy: New α-synuclein partners in glial cytoplasmic inclusions implicated in the disease pathogenesis.
Bettencourt C, Miki Y, Piras IS, de Silva R, Foti SC, Talboom JS, Revesz T, Lashley T, Balazs R, Viré E, et al. Neuropathol Appl Neurobiol. 2021 Aug; 47(5):640-652. Epub 2021 Jan 19.

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the MOBP gene.
RefSeq protein product
See the reference protein sequence for myelin-associated oligodendrocyte basic protein isoform a (NP_001265251.1).

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Protein sequence from Nucleotide coding region
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Nucleotide