Gene table: search width pubmed_id = 9916797


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Primary systemic carnitine deficiency - (AR)
9.18
9916797
SLC22A5 (5q31)
Solute carrier family 22 member 5
* Carnitine deficiency, systemic primary - CDSP