Gene symbol and protein | Gene Location | All allelic disease phenotypes - locus/disease symbols |
SLC22A5 Solute carrier family 22 member 5       | 5q31 | * Carnitine deficiency, systemic primary - CDSP (9.19) |
This table has been prepared by Dr Gisèle Bonne * - PhD and by Pr. François Rivier ** - MD, PhD
This website is developed and maintained by Dalil Hamroun** - PhD
* Sorbonne Université-Inserm, Centre of Research in Myology , Paris, France.
** Chu de Montpellier, Montpellier. France.
GT_NMD 2024 (updated 17/01/2024)
Gene symbol and protein | Gene Location | All allelic disease phenotypes - locus/disease symbols |
SLC22A5 Solute carrier family 22 member 5 | 5q31 | * Carnitine deficiency, systemic primary - CDSP (9.19) |