ATPase subunit alpha-2 is a protein which in humans is encoded by the ATP1A2 gene. The protein encoded by this gene belongs to the family of P-type cation...
11 KB (1,269 words) - 20:31, 22 October 2023
Familial hemiplegic migraine (section FHM2 (ATP1A2))
less than 25% of cases, is caused by mutations in the Na+ /K+ -ATPase gene ATP1A2. FHM3 is a rare subtype of FHM and is caused by mutations in a sodium channel...
41 KB (4,222 words) - 16:24, 26 April 2024
suffer from Hemiplegic migraines may have mutations of the CACNA1A and the ATP1A2 genes. The ICHD classification and diagnosis of migraine distinguish 6 subtypes...
7 KB (691 words) - 09:11, 19 June 2024
usually take two main conformations, E1 and E2. Na+/K+ transporting: ATP1A1, ATP1A2, ATP1A3, ATP1A4, ATP1B1, ATP1B2, ATP1B3, ATP1B4 Ca++ transporting: ATP2A1...
18 KB (2,106 words) - 04:39, 11 July 2024
K+-ATPase." Alpha: ATP1A1, ATP1A2, ATP1A3, ATP1A4. ATP1A1 is expressed ubiquitously in vertebrates, and ATP1A3 in neural tissue. ATP1A2 is also known as "alpha(+)"...
38 KB (4,367 words) - 16:52, 26 June 2024
HGNC:25666 Q7L5A3 1222 ATOX1 HGNC:798 O00244 1223 ATP1A1 HGNC:799 P05023 1224 ATP1A2 HGNC:800 P50993 1225 ATP1A3 HGNC:801 P13637 1226 ATP1A4 HGNC:14073 Q13733...
277 KB (17 words) - 18:34, 6 October 2024
ATP1A3. A small number of cases seem to be caused by a mutation in the ATP1A2 gene. Where the mutation is inherited, it has the autosomal dominant pattern...
25 KB (2,582 words) - 12:12, 13 July 2024
cases with permanent neurological deficits have also been noted. CACNA1A, ATP1A2 and SCNA1 are genes associated with hemipeligic migraines, although many...
5 KB (444 words) - 16:35, 17 August 2023
Ca2+ ATPase: ATP2B1, ATP2B2, ATP2B3, ATP2B4 P2C: Na+/K+ ATPase: ATP1A1, ATP1A2, ATP1A3, ATP1A4, ATP1B1, ATP1B2, ATP1B3, ATP1B4 P2C: H+/K+ ATPase, gastric:...
42 KB (5,160 words) - 12:04, 17 June 2024
childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2". Neuropediatrics. 35 (5): 293–6. doi:10.1055/s-2004-821082. PMID 15534763...
12 KB (1,434 words) - 08:49, 31 July 2024
Alström syndrome; 203800; ALMS1 Alternating hemiplegia of childhood; 104290; ATP1A2 Alveolar capillary dysplasia with misalignment of pulmonary veins; 265380;...
234 KB (18,877 words) - 15:43, 9 May 2024
"Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4". Headache. 46 (7): 1136–41. doi:10.1111/j.1526-4610...
9 KB (1,221 words) - 18:33, 22 August 2024