Homo sapiens CCM2 scaffold protein (CCM2), transcript variant 6, mRNA

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Loss of heterozygosity in CCM2 cDNA revealing a structural variant causing multiple cerebral cavernous malformations. [Eur J Hum Genet. 2024]
Loss of heterozygosity in CCM2 cDNA revealing a structural variant causing multiple cerebral cavernous malformations.
Chaussenot A, Ayrignac X, Chatron N, Granchon-Riolzir T, Labauge P, Tournier-Lasserve E, Riant F. Eur J Hum Genet. 2024 Jul; 32(7):876-878. Epub 2024 May 16.
Convergence of coronary artery disease genes onto endothelial cell programs. [Nature. 2024]
Convergence of coronary artery disease genes onto endothelial cell programs.
Schnitzler GR, Kang H, Fang S, Angom RS, Lee-Kim VS, Ma XR, Zhou R, Zeng T, Guo K, Taylor MS, et al. Nature. 2024 Feb; 626(8000):799-807. Epub 2024 Feb 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 14 reference mRNA sequence splice variants for the CCM2 gene.
RefSeq protein product
See the reference protein sequence for cerebral cavernous malformations 2 protein isoform 5 (NP_001350387.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide