Homo sapiens methylmalonic aciduria (cobalamin deficiency) cblA type, - Nucleotide

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TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing. [Neuro Oncol. 2023]
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing.
Demirdizen E, Al-Ali R, Narayanan A, Sun X, Varga JP, Steffl B, Brom M, Krunic D, Schmidt C, Schmidt G, et al. Neuro Oncol. 2023 Jun 2; 25(6):1031-1043.
Ocular manifestations in patients with inborn errors of intracellular cobalamin metabolism: a systematic review. [Hum Genet. 2022]
Ocular manifestations in patients with inborn errors of intracellular cobalamin metabolism: a systematic review.
Matmat K, Guéant-Rodriguez RM, Oussalah A, Wiedemann-Fodé A, Dionisi-Vici C, Coelho D, Guéant JL, Conart JB. Hum Genet. 2022 Jul; 141(7):1239-1251. Epub 2021 Oct 15.
Unbiased Profiling of the Human Proinsulin Biosynthetic Interaction Network Reveals a Role for Peroxiredoxin 4 in Proinsulin Folding. [Diabetes. 2020]
Unbiased Profiling of the Human Proinsulin Biosynthetic Interaction Network Reveals a Role for Peroxiredoxin 4 in Proinsulin Folding.
Tran DT, Pottekat A, Mir SA, Loguercio S, Jang I, Campos AR, Scully KM, Lahmy R, Liu M, Arvan P, et al. Diabetes. 2020 Aug; 69(8):1723-1734. Epub 2020 May 26.

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the MMAA gene.

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Nucleotide