Homo sapiens coiled-coil and C2 domain containing 2A (CC2D2A), transcr - 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.

RefSeq protein product
See the reference protein sequence for coiled-coil and C2 domain-containing protein 2A isoform a (NP_001365544.1).

Protein
Protein sequence from Nucleotide coding region
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Chromosome neighbors for GEO Profiles (Select 121492014) (16)
GEO Profiles
Chromosome neighbors for GEO Profiles (Select 121485569) (15)
GEO Profiles
Taxonomy Links for Nucleotide (Select 187460) (1)
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Gene Links for GEO Profiles (Select 121471034) (14)
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Genome Links for Taxonomy (Select 5476) (1)
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Nucleotide