Homo sapiens mRNA for KIAA1161 protein, partial cds

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Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implications. [Acta Neuropathol Commun. 2024]
Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implications.
Hobara T, Higuchi Y, Yoshida M, Suehara M, Ando M, Yuan JH, Yoshimura A, Kojima F, Matsuura E, Okamoto Y, et al. Acta Neuropathol Commun. 2024 Aug 23; 12(1):136. Epub 2024 Aug 23.
Fahr's disease linked to a novel mutation in MYORG variants manifesting as paroxysmal limb stiffness and dysarthria: Case report and literature review. [Mol Genet Genomic Med. 2023]
Fahr's disease linked to a novel mutation in MYORG variants manifesting as paroxysmal limb stiffness and dysarthria: Case report and literature review.
Zhao T, Xu S, Liu S, Xu J, Zhang X, Zhan Y. Mol Genet Genomic Med. 2023 Dec; 11(12):e2276. Epub 2023 Sep 7.
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.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the MYORG gene.

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Nucleotide