calcium channel, voltage-dependent, alpha 2/delta subunit 2, isoform C - Protein

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Epileptic Encephalopathy and Cerebellar Atrophy Resulting from Compound Heterozygous CACNA2D2 Variants. [Case Rep Genet. 2018]
Epileptic Encephalopathy and Cerebellar Atrophy Resulting from Compound Heterozygous CACNA2D2 Variants.
Butler KM, Holt PJ, Milla SS, da Silva C, Alexander JJ, Escayg A. Case Rep Genet. 2018; 2018:6308283. Epub 2018 Oct 15.
Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies. [Genet Med. 2019]
Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies.
Valence S, Cochet E, Rougeot C, Garel C, Chantot-Bastaraud S, Lainey E, Afenjar A, Barthez MA, Bednarek N, Doummar D, et al. Genet Med. 2019 Mar; 21(3):553-563. Epub 2018 Jul 12.
CACNA2D2 promotes tumorigenesis by stimulating cell proliferation and angiogenesis. [Oncogene. 2015]
CACNA2D2 promotes tumorigenesis by stimulating cell proliferation and angiogenesis.
Warnier M, Roudbaraki M, Derouiche S, Delcourt P, Bokhobza A, Prevarskaya N, Mariot P. Oncogene. 2015 Oct 16; 34(42):5383-94. Epub 2015 Jan 26.

RefSeq genomic sequence
See the genomic reference sequence for the CACNA2D2 gene (NG_034070.1).
RefSeq protein isoforms
See 7 reference sequence protein isoforms for the CACNA2D2 gene.

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CCT6B chaperonin containing TCP1 subunit 6B [Homo sapiens]
CCT6B chaperonin containing TCP1 subunit 6B [Homo sapiens]
Gene ID:10693

Gene
Gm15636 predicted gene 15636 [Mus musculus]
Gm15636 predicted gene 15636 [Mus musculus]
Gene ID:100416442

Gene
related_functional_gene_57784[group] AND (alive[prop]) (1)
Gene
1699181[uid] (1)
Taxonomy
Metagenome-Assembled Genome: ERR9578258_bin.36_MetaWRAP_v1.3_MAG
Metagenome-Assembled Genome: ERR9578258_bin.36_MetaWRAP_v1.3_MAG

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Protein