Homo sapiens coiled-coil and C2 domain containing 2A (CC2D2A), RefSeqG - Nucleotide

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Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome. [Genes (Basel). 2023]
Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome.
Cabrita Pinto RL, Viaggi S, Canale E, Martinez Popple M, Capra V, Conteduca G, Testa B, Coviello D, Covone AE. Genes (Basel). 2023 Mar 28; 14(4). Epub 2023 Mar 28.
New insights into CC2D2A-related Joubert syndrome. [J Med Genet. 2023]
New insights into CC2D2A-related Joubert syndrome.
Harion M, Qebibo L, Riquet A, Rougeot C, Afenjar A, Garel C, Louha M, Lacaze E, Audic-Gérard F, Barth M, et al. J Med Genet. 2023 Jun; 60(6):578-586. Epub 2022 Nov 1.
In-Depth In Vivo Crosslinking in Minutes by a Compact, Membrane-Permeable, and Alkynyl-Enrichable Crosslinker. [Anal Chem. 2022]
In-Depth In Vivo Crosslinking in Minutes by a Compact, Membrane-Permeable, and Alkynyl-Enrichable Crosslinker.
Gao H, Zhao L, Zhong B, Zhang B, Gong Z, Zhao B, Liu Y, Zhao Q, Zhang L, Zhang Y. Anal Chem. 2022 May 31; 94(21):7551-7558. Epub 2022 May 16.

RefSeq alternative splicing
See 11 reference mRNA sequence splice variants for the CC2D2A gene.

Protein
Protein sequence from Nucleotide coding region
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RNA
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Nucleotide