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.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.

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Protein sequence from Nucleotide coding region
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Nucleotide