Homo sapiens coiled-coil and C2 domain containing 2B (CC2D2B), transcr - Nucleotide

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The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency. [Gene. 2024]
The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency.
Rupar N, Šelb J, Košnik M, Zidarn M, Andrejević S, Čulav L, Grivčeva-Panovska V, Korošec P, Rijavec M. Gene. 2024 Aug 15; 919:148496. Epub 2024 Apr 27.
Cross-linking mass spectrometry discovers, evaluates, and corroborates structures and protein-protein interactions in the human cell. [Proc Natl Acad Sci U S A. 2023]
Cross-linking mass spectrometry discovers, evaluates, and corroborates structures and protein-protein interactions in the human cell.
Bartolec TK, Vázquez-Campos X, Norman A, Luong C, Johnson M, Payne RJ, Wilkins MR, Mackay JP, Low JKK. Proc Natl Acad Sci U S A. 2023 Apr 25; 120(17):e2219418120. Epub 2023 Apr 18.
Ovarian tumorB1-mediated heat shock transcription factor 1 deubiquitination is critical for glycolysis and development of endometriosis. [iScience. 2022]
Ovarian tumorB1-mediated heat shock transcription factor 1 deubiquitination is critical for glycolysis and development of endometriosis.
Ling X, Lu J, Wang X, Liu L, Liu L, Wang Y, Sun Y, Ren C, Lu C, Yu Z. iScience. 2022 Nov 18; 25(11):105363. Epub 2022 Oct 14.

RefSeq alternative splicing
See 32 reference mRNA sequence splice variants for the CC2D2B gene.
RefSeq protein product
See the reference protein sequence for protein CC2D2B isoform 3 (NP_001335937.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide