Homo sapiens gap junction protein gamma 2 (GJC2), RefSeqGene on chromo - Nucleotide

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Mechanisms of Diseases Associated with Mutation in GJC2/Connexin 47. [Biomolecules. 2023]
Mechanisms of Diseases Associated with Mutation in GJC2/Connexin 47.
Abrams CK. Biomolecules. 2023 Apr 21; 13(4). Epub 2023 Apr 21.
Lack of embryonic homozygous or adult heterozygous lymphatic phenotypes for a Sos1 mutation and lack of lymphatic embryonic phenotypes for a homozygous Cx47 mutation in mice. [Lymphology. 2022]
Lack of embryonic homozygous or adult heterozygous lymphatic phenotypes for a Sos1 mutation and lack of lymphatic embryonic phenotypes for a homozygous Cx47 mutation in mice.
Geng X, Chen L, Srinivasan RS, Kylat RJ, Witte MH, Erickson RJ. Lymphology. 2022; 55(3):129-134.
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.

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Protein sequence from Nucleotide coding region
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PREDICTED: Homo sapiens ubiquitin specific peptidase 36 (USP36), transcript vari...
PREDICTED: Homo sapiens ubiquitin specific peptidase 36 (USP36), transcript variant X14, mRNA
gi|2462556621|ref|XM_054316774.1|

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Nucleotide