CACNA1A articles on Wikipedia
Cav2.1
The Cav2.1 P/Q voltage-dependent calcium channel is encoded by the CACNA1A gene. Voltage-dependent calcium channels mediate the entry of calcium ions
Jun 8th 2016



CACNA1I
type, alpha 1I subunit, also known as CACNA1I or Cav3.3 is a protein which in humans is encoded by the CACNA1I gene. Voltage-dependent calcium channels
Feb 6th 2017



CACNA1G
type, alpha 1G subunit, also known as CACNA1G or Cav3.1 is a protein which in humans is encoded by the CACNA1G gene. Voltage-dependent calcium channels
Feb 6th 2017



CACNA2D1
Voltage-dependent calcium channel subunit alpha-2/delta-1 is a protein that in humans is encoded by the CACNA2D1 gene. This gene encodes a member of the
Feb 6th 2017



Cav1.4
known as the calcium channel, voltage-dependent, L type, alpha 1F subunit (CACNA1F), is a human gene. This gene encodes a member of the alpha-1 subunit family;
May 22nd 2016



CACNA1H
voltage-dependent, T type, alpha 1H subunit, also known as CACNA1H, is a protein which in humans is encoded by the CACNA1H gene. This gene encodes Cav3.2, a T-type
Feb 6th 2017



CACNA2D2
Voltage-dependent calcium channel subunit alpha2delta-2 is a protein that in humans is encoded by the CACNA2D2 gene. This gene encodes a member of the
Feb 6th 2017



Cav1.1
voltage-dependent, L type, alpha 1S subunit, (CACNA1S), is a protein which in humans is encoded by the CACNA1S gene. It is also known as CACNL1A3 and the
May 19th 2016



Cav1.2
subunit (also known as Cav1.2) is a protein that in humans is encoded by the CACNA1C gene. Cav1.2 is a subunit of L-type voltage-dependent calcium channel.
Apr 4th 2017



CACNA2D3
Calcium channel, voltage-dependent, alpha 2/delta subunit 3 is a protein that in humans is encoded by the CACNA2D3 gene on chromosome 3 (locus 3p21.1)
Feb 6th 2017



Cav1.3
subunit (also known as Cav1.3) is a protein that in humans is encoded by the CACNA1D gene. Cav1.3 channels belong to the Cav1 family, which form L-type calcium
Nov 30th 2016



R-type calcium channel
voltage-dependent, R type, alpha 1E subunit (CACNA1E) or Cav2.3 which in humans is encoded by the CACNA1E gene. They are strongly expressed in cortex
Apr 24th 2017



Episodic ataxia
stress, but also by coffee and alcohol. EA2 is caused by mutations in CACNA1A, which encodes the P/Q-type voltage-gated calcium channel CaV2.1, and is
Mar 4th 2017



Familial hemiplegic migraine
mutations in a gene coding for the P/Q-type calcium channel α subunit, CACNA1A. FHM1 is also associated with cerebellar degeneration. FHM2, which accounts
Mar 16th 2017



L-type calcium channel
subunits make up the selectivity filter. CACNA1C, CACNA1D, CACNA1S, CACNA1F CACNA1C CACNA1D CACNA1S CACNA1F Felizola SJ, Maekawa T, Nakamura Y, Satoh
Apr 24th 2017



CACNA2D4
Calcium channel, voltage-dependent, alpha 2/delta subunit 4 is a protein that in humans is encoded by the CACNA2D4 gene. This gene encodes a member
Feb 6th 2017



CACNA1B
channel subunit alpha-1B is a protein that in humans is encoded by the CACNA1B gene. "Drugs that physically interact with Calcium voltage-gated channel
Apr 6th 2017



1I
refer to: 1i Productions, an American board game publisher SSH 1I (WA), part of which became Washington State Route 525 CACNA1I I1 (disambiguation) pppr
Nov 27th 2016



N-type calcium channel
For example, mutations in the CACNA1B gene have been associated with Myoclonus-Dystonia syndrome . Duplication of the CACNA1B gene has also been linked to
Apr 26th 2017



Spinocerebellar ataxia type 6
phenotypic overlap between the two disorders. SCA6 is caused by mutations in CACNA1A, a gene encoding a calcium channel α subunit. These mutations tend to be
Jun 21st 2016



X-linked congenital stationary night blindness
formation or synaptic transmission. CSNB2 is caused by mutations in the gene CACNA1F, which encodes a voltage-gated calcium channel CaV1.4. Not all Congenital
Jun 21st 2016



Childhood absence epilepsy
T-type calcium channels such as those encoded by CACNA1H. There are currently 20 mutations in CACNA1H associated with CAE. These mutations are likely
Mar 4th 2017



Calcium-binding protein 1
also interacts with CACNA1ACACNA1A in the pre and post synaptic membranes via C-terminal calcium binding motif. It also interacts with CACNA1C via C-terminal C
Nov 24th 2016



Ion channel family
MCOLN2; MCOLN3; TRPA1 PKD1L3; CACNA1A; CACNA1B; CACNA1C; CACNA1D; CACNA1E; CACNA1F; CACNA1G; CACNA1H; CACNA1I; CACNA1S CATSPER1; CATSPER2; CATSPER3;
Aug 13th 2016



Voltage-dependent calcium channel
("Purkinje") /Q-type calcium channel HVA (high voltage activated) Cav2.1 (CACNA1A) α2δ, β, possibly γ Purkinje neurons in the cerebellum / Cerebellar granule
Mar 10th 2017



P-type calcium channel
channels of skeletal muscles. The α1 subunit is encoded specifically by the CACNA1A gene and is composed of four domains, each containing six transmembrane
Apr 24th 2017



Timothy syndrome
caused by mutations in CACNA1C, the gene encoding the calcium channel Cav1.2 α subunit. Timothy syndrome mutations in CACNA1C cause delayed channel closing
Mar 28th 2017



Ocular albinism
41-50. Jalkanen R, Bech-Hansen NT, Tobias R, et al. (June 2007). "A novel CACNA1F gene mutation causes Aland Island eye disease". Invest. Ophthalmol. Vis
May 24th 2016



Von Willebrand factor type A domain
The von Willebrand factor is a large multimeric glycoprotein found in blood plasma. Mutant forms are involved in the aetiology of bleeding disorders. In
Jun 6th 2016



Lucid interval
"Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic
Feb 22nd 2017



CACNB4
(2006). "Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4.". Headache. 46 (7): 1136–41. doi:10.1111/j
Feb 6th 2017



Chromosome 19 (human)
kinase 11 (PeutzPeutz-Jeghers syndrome) ZNF649: Transcriptional suppressor CACNA1A: Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit (Familial
Mar 26th 2017



Sophia Frangou
Tatarelli, R.; Girardi, P.; Collier, D.; Frangou, S. (2011). "The impact of the CACNA1C gene polymorphism on frontolimbic function in bipolar disorder". Mol Psychiatry
Nov 2nd 2016



Index of biophysics articles
Matthews (biochemist) Britton Chance Brush border Bulk movement CACNA1G CACNA1H CACNA1I CACNA2D1 CACNA2D2 CACNB1 CACNB2 CACNB3 CACNB4 CACNG1 CACNG2 CACNG3
Aug 14th 2014



Hypokalemic periodic paralysis
the channels cannot open normally. In patients with mutations in SCN4A or CACNA1S, therefore, the channel has a reduced excitability and signals from the
Mar 31st 2017



Endophenotype
anterior cingulate cortex, striatum, and amygdala. A polymorphism in the CACNA1C gene coding for the voltage-dependent calcium channel Cav1.2 has been found
Mar 19th 2017



Nyctalopin
PMID 12506099.  Zito I, Allen LE, Patel RJ, et al. (2003). "MutationsMutations in the CACNA1F and NYX genes in British CSNBX families.". Hum. Mutat. 21 (2): 169. doi:10
Jul 30th 2016



Chromosome 3 (human)
Chromosome 3 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 3 spans almost 200 million
Apr 26th 2017



Ankyrin
"Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder". Nat. Genet. 40 (9): 1056–8. doi:10.1038/ng.209. PMC 2703780
Dec 6th 2016



Ribbon synapse
X-linked congenital stationary night blindness (CSNB) through mutations in the CACNA1F gene, which codes for the αF1-subunit of the L-type calcium channel Cav1
Apr 25th 2017



Pamela Sklar
(ANK3) and the alpha-1C subunit of the L-type voltage-gated calcium channel (CACNA1C) in bipolar disorder. Nat Genet 40:1056-8. International Schizophrenia
Feb 22nd 2017



Idiopathic generalized epilepsy
unconsciousness (absence). Mutations in the calcium channel α subunit encoding gene CACNA1H and the GABA receptor γ subunit encoding gene GABRG2 yield susceptibility
Feb 19th 2017



Nystagmus
mutations are found in NYX (nyctalopin). CSNB-2 involves mutations of CACNA1F, a voltage-gated calcium channel that, when mutated, does not conduct ions
Apr 24th 2017



Brugada syndrome
Antzelevitch has identified mutations in the L-type calcium channel subunits (CACNA1C (A39V and G490R) and CACNB2 (S481L)) leading to ST elevation and a relatively
Apr 18th 2017



Long QT syndrome
syndrome is due to mutations in the calcium channel Cav1.2 encoded by the gene CACNA1c. Since the calcium channel Cav1.2 is abundant in many tissues, patients
Apr 24th 2017



Li Tao (psychologist)
Zhiqiang; Chen, JianhuaJianhua; Li, Wenjin; Wang, Ti; Ji, Jue (2014-01-01). "CACNA1C, schizophrenia and major depressive disorder in the Han Chinese population"
Apr 4th 2017



ANK3
"Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder". Nat. Genet. 40 (9): 1056–8. doi:10.1038/ng.209. PMC 2703780
Mar 28th 2017



Pleiotropy
involved in calcium channel signaling with neurons. One of these genes, CACNA1C, has been found to influence cognition. It has been associated with autism
Apr 18th 2017



Malignant hyperthermia
phosphate and creatine kinase. The other known causative gene for MH is CACNA1S, which encodes an L-type voltage-gated calcium channel α-subunit. There
Apr 28th 2017



Physical exercise
"Workout" and "Exercise" redirect here. For other uses, see Workout (disambiguation) and Exercise (disambiguation). Physical exercise is any
Apr 25th 2017





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