CACNA1D Gene - GeneCards | CAC1D Protein | CAC1D Antibody
2024年12月24日 · CACNA1D (Calcium Voltage-Gated Channel Subunit Alpha1 D) is a Protein Coding gene. Diseases associated with CACNA1D include Sinoatrial Node Dysfunction And …
A Review of the CACNA Gene Family: Its Role in Neurological …
The CACNA1D gene encodes calcium voltage-gated channel subunit alpha1 D, or subunit Cav1.3, primarily found in the postsynaptic regions of the brain (dendritic spines), inner hair …
钙电压门控通道亚基 alpha1 D（CACNA1D）基因 | MCE
钙通道类型的独特特性主要与各种 alpha-1 亚型 (即 alpha-1A、B、C、D、E 和 S) 的表达有关。 该基因编码 alpha-1D 亚基。 已发现该基因编码不同亚型的几种转录变体。 [RefSeq 提 …
CACNA1D gene - MedlinePlus
These channels transport positively charged calcium atoms (calcium ions) across cell membranes. The CACNA1D gene provides instructions for making one part (the alpha-1 …
CACNA1D calcium voltage-gated channel subunit alpha1 D
2025年2月8日 · CACNA1D mutations predominate in small zona glomerulosa (ZG)-like Aldosterone-producing Adenomas. The CACNA1C-L762F mutation is associated with …
CACNA1D overexpression and voltage-gated calcium channels in …
2023年3月22日 · CACNA1D, encoding Ca V 1.3 ion channels is upregulated in prostate cancer. Here we show how hormone therapy affects CACNA1D expression and Ca V 1.3 function. …
Somatic and germline CACNA1D calcium channel mutations in …
CACNA1D encodes the pore-forming α 1 subunit of a voltage-gated calcium channel. These channels feature four homologous repeats (I–IV) with 6 transmembrane segments (S1-S6) …
Cacna1d calcium channel, voltage-dependent, L type, alpha 1D …
Gene ID: 12289, updated on 13-Jan-2025. This gene encodes a pore-forming subunit of the L-type, voltage-activated calcium channel family. These channels have been found to play a role …
CACNA1D calcium voltage-gated channel subunit alpha1 D …
2023年11月23日 · Voltage-dependent calcium channels mediate the entry of calcium ions into excitable cells, and are also involved in a variety of calcium-dependent processes, including …
Pathogenicity of de novo CACNA1D Ca2+ channel variants
2024年3月29日 · De novo missense mutations in the gene of their pore-forming α1-subunit (CACNA1D) induce severe gating defects which lead to autism spectrum disorder and a more …