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Results 1 - 7 of 7 for CACNA1A
  1. CACNA1A gene 
    The CACNA1A gene belongs to a family of genes that provide instructions for making calcium channels. These channels, which transport positively charged calcium ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
  2. Sporadic hemiplegic migraine 
    ... sporadic hemiplegic migraine). Mutations in the ATP1A2 and CACNA1A genes have been found to cause sporadic hemiplegic ... by neighboring neurons. Mutations in the ATP1A2 and CACNA1A genes disrupt the transport of ions in neurons, ...
    https://medlineplus.gov/.../condition/sporadic-hemiplegic-migraine - Genetics
  3. Spinocerebellar ataxia type 6 
    ... individuals. Variants (also known as mutations) in the CACNA1A gene cause SCA6. The CACNA1A gene provides instructions for making a protein that ... and other parts of the nervous system. The CACNA1A gene provides instructions for making one part (the ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-6 - Genetics
  4. Familial hemiplegic migraine 
    ... females more often than males. Mutations in the CACNA1A, ATP1A2, SCN1A, and PRRT2 genes have been found ... neighboring neurons. Researchers believe that mutations in the CACNA1A, ATP1A2, and SCN1A genes can upset the balance ...
    https://medlineplus.gov/.../condition/familial-hemiplegic-migraine - Genetics
  5. Episodic ataxia 
    ... potassium ions, and the protein produced from the CACNA1A gene transports calcium ions. The movement of these ... the nervous system. Variants in the KCNA1 and CACNA1A genes cause episodic ataxia types 1 and 2, ...
    https://medlineplus.gov/genetics/condition/episodic-ataxia - Genetics
  6. 19p13.13 deletion syndrome 
    ... For example, studies suggest that deletion of the CACNA1A gene may cause seizures in affected individuals. Researchers ... to the other specific features of the disorder. CACNA1A CALR chromosome 19 Additional Information from NCBI Gene: ...
    https://medlineplus.gov/genetics/condition/19p1313-deletion-syndrome - Genetics
  7. ATP1A2 gene 
    ... Lasserve E. De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine. ...
    https://medlineplus.gov/genetics/gene/atp1a2 - Genetics