Browse our CACNA1S Proteins (CACNA1S)

Full name:
Calcium Channel, Voltage-Dependent, L Type, alpha 1S Subunit Proteins (CACNA1S)
On www.antibodies-online.com are 6 Calcium Channel, Voltage-Dependent, L Type, alpha 1S Subunit (CACNA1S) Proteins from 3 different suppliers available. Additionally we are shipping CACNA1S Antibodies (57) and CACNA1S Kits (4) and many more products for this protein. A total of 67 CACNA1S products are currently listed.
Synonyms:
AW493108, ca(v)1.1, CACNA1S, CACNL1A3, caV1.1, Cchl1a3, fmd, HOKPP, HOKPP1, hypoPP, mdg, MHS5, sj, TTPP1
list all proteins Gene Name GeneID UniProt
CACNA1S 779 Q13698
CACNA1S 12292  
Rat CACNA1S CACNA1S 682930  

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CACNA1S Proteins (CACNA1S) by Origin

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More Proteins for CACNA1S Interaction Partners

Human Calcium Channel, Voltage-Dependent, L Type, alpha 1S Subunit (CACNA1S) interaction partners

  1. whole-exome next-generation sequencing was used to identify a mutation in the CACNA1S gene, R900S, which is a rare mutation associated with hypokalemic periodic paralysis; study provides further evidence for the phenotypic variation and pharmacogenomics of hypokalemic periodic paralysis

  2. These results provide new insights into the role of muscle-specific (show EIF3K Proteins) proteins on the structural arrangement of alpha1S intracellular loops and point to a new conformational effect of the beta1a subunit in supporting skeletal muscle excitation-contraction coupling.

  3. CACNA1S and SCN4A (show SCN4A Proteins) mutations are relatively rare in patients with hypokalemic periodic paralysis

  4. The authors found one and three rare variants of unknown significance in CACNA1S in the Malignant Hyperthermia and Exertional Heat cohorts

  5. Defects in the genes coding for the skeletal muscle ryanodine receptor (show RYR1 Proteins) and alpha 1 subunit of the dihydropyridine receptor (CACNA1S) have been identified as causative for malignant hyperthermia.

  6. Aberrant splicing of Cav (show CA5A Proteins) 1.1 may alter intracellular Ca(2 (show CA2 Proteins)+) signalling in myotonic dystrophy 1 and 2 myotubes. The differing dysregulation of intracellular Ca(2 (show CA2 Proteins)+) handling in DM1 (show DMPK Proteins) and DM2 (show CNBP Proteins) may explain their distinct sarcolemmal hyperexcitabilities.

  7. Exome sequencing revealed one rare cacna1s nonsynonymous variant in a family with malignant hyperthermia

  8. Data indicate that the presence of either one of these JP-45 (show JSRP1 Proteins) variants decreased the sensitivity of the dihydropyridine receptor DHPR (show QDPR Proteins) to activation.

  9. Affected members of a 5-generation Chinese family with hypokalemic periodic paralysis patients had a novel His916Gln mutation in all male HypoPP patients of the family. Penetrance of the mutation was complete in male carriers, but not female carriers.

  10. Misregulated splicing and altered gating of Ca(V)1.1 calcium channel is associated with muscle weakness in myotonic dystrophy.

Mouse (Murine) Calcium Channel, Voltage-Dependent, L Type, alpha 1S Subunit (CACNA1S) interaction partners

  1. TnT3 regulates transcription of Cacna1s, the gene encoding Cav1.1. Knocking down TnT3 in vivo downregulated Cav1.1.

  2. mutating residue E4242 affects RyR1 (show RYR1 Proteins) structures critical for retrograde communication with CaV1.1

  3. These results provide new insights into the role of muscle-specific (show EIF3K Proteins) proteins on the structural arrangement of alpha1S intracellular loops and point to a new conformational effect of the beta1a subunit in supporting skeletal muscle excitation-contraction coupling.

  4. Events occurring locally in the skeletal muscle of SOD1 mutant mice contribute to the impairment of CaV1.1 function in ALS muscle independently of innervation status.

  5. Knockdown of Cav1.1 channels in T cells abrogated calcium entry after TCR stimulation, suggesting that Cav1.1 channels are controlled by T cell receptor signaling

  6. Treatment of MSC (show MSC Proteins) with BMP4 (show BMP4 Proteins) caused a significant increase in expression of Cav1.2 (show CACNA1C Proteins), a delay in expression of Cav1.1, and a reduction in the duration of calcium transients when extracellular calcium was removed

  7. This study delineates a previously uncharacterized CaV1.1-mediated pathway that regulates energy utilization in skeletal muscle.

  8. Raptor (show RPTOR Proteins) ablation in skeletal muscle decreases Cav1.1 expression and affects the function of the excitation-contraction coupling supramolecular complex.

  9. amino-termini of Rad and Rem (show REM1 Proteins) as the structural elements dictating the specific modes of inhibition of CaV1.1

  10. the localization and stability of Cacna1s depend on the expression of mGluR6 (show GRM6 Proteins) and its cascade components, and they suggest that Cacna1s is part of the mGluR6 (show GRM6 Proteins) complex.

CACNA1S Protein Profile

Protein Summary

This gene encodes one of the five subunits of the slowly inactivating L-type voltage-dependent calcium channel in skeletal muscle cells. Mutations in this gene have been associated with hypokalemic periodic paralysis, thyrotoxic periodic paralysis and malignant hyperthermia susceptibility.

Alternative names and synonyms associated with CACNA1S

  • calcium channel, voltage-dependent, L type, alpha 1S subunit (CACNA1S)
  • calcium channel, voltage-dependent, L type, alpha 1S subunit (cacna1s)
  • calcium channel, voltage-dependent, L type, alpha 1S subunit (Cacna1s)
  • AW493108 protein
  • ca(v)1.1 protein
  • CACNA1S protein
  • CACNL1A3 protein
  • caV1.1 protein
  • Cchl1a3 protein
  • fmd protein
  • HOKPP protein
  • HOKPP1 protein
  • hypoPP protein
  • mdg protein
  • MHS5 protein
  • sj protein
  • TTPP1 protein

Protein level used designations for CACNA1S

calcium channel, voltage-dependent, L type, alpha 1S subunit , voltage-dependent L type calcium channel alpha 1S subunit , voltage-dependent L-type calcium channel subunit alpha-1S , transverse tubule dihydropyridine receptor alpha 1 subunit , calcium channel, L type, alpha 1 polypeptide, isoform 3 (skeletal muscle, hypokalemic periodic paralysis) , dihydropyridine receptor , dihydropyridine-sensitive L-type calcium channel alpha-1 subunit , voltage-gated calcium channel subunit alpha Cav1.1 , calcium channel, L type, alpha-1 polypeptide, isoform 3, skeletal muscle , DHPR alpha1s , dihydropyridine receptor alpha 1S , muscle dysgenesis , ROB1 , L-type calcium channel, alpha 1 subunit , voltage-gated calcium channel alpha 1S subunit

GENE ID SPECIES
469635 Pan troglodytes
490244 Canis lupus familiaris
654399 Felis catus
100034092 Equus caballus
100381134 Xenopus laevis
100734741 Cavia porcellus
779 Homo sapiens
100009585 Oryctolagus cuniculus
12292 Mus musculus
682930 Rattus norvegicus
395985 Gallus gallus
100286866 Sus scrofa
100337204 Bos taurus
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