rt1-da
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  • Official Full Name
  • RT1 class II, locus Da
  • Background
  • This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing of this gene results in three transcript variants that encode the same protein.
  • Synonyms
  • RT1-DA; RT1 class II, locus Da; H2-Ea; Histocompatibility 2, class II antigen E alpha; MGC112637; MHC class II antigen RT1.D alpha chain; MHC class II RT1D alpha chain antigen; MHC RT1.u D alpha chain; RT1 class II, locus Da; RT1 D alpha; RT1 Du alpha; RT1-u; RT1-D alpha; RT1-Du alpha; MHC RT1.u-D-alpha chain; MHC class II RT1D alpha chain antigen; MHC class II antigen RT1.D alpha chain; histocompatibility 2, class II antigen E alpha; H2-Ea; RT1-u

RT1-DA Related Articles

Almeida-Suhett, CP; Li, Z; et al. Temporal Course of Changes in Gene Expression Suggests a Cytokine-Related Mechanism for Long-Term Hippocampal Alteration after Controlled Cortical Impact. JOURNAL OF NEUROTRAUMA 31:683-690(2014).
Grieb, B; Engler, G; et al. High-Frequency Stimulation of the Subthalamic Nucleus Counteracts Cortical Expression of Major Histocompatibility Complex Genes in a Rat Model of Parkinson's Disease. PLOS ONE 9:-(2014).