KEGG   VARIANT: 6584v1
Entry
6584v1                      Variant                                
Name
SLC22A5 mutation
Type
Loss of function
Gene
SLC22A5  organic cation/carnitine transporter 2 isoform b [KO:K08202]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 603377
Network
nt06020  beta-Oxidation in mitochondria
Disease
H01589  Systemic primary carnitine deficiency
Reference
PMID:9916797
  Authors
Nezu J, Tamai I, Oku A, Ohashi R, Yabuuchi H, Hashimoto N, Nikaido H, Sai Y, Koizumi A, Shoji Y, Takada G, Matsuishi T, Yoshino M, Kato H, Ohura T, Tsujimoto G, Hayakawa J, Shimane M, Tsuji A
  Title
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter.
  Journal
Nat Genet 21:91-4 (1999)
DOI:10.1038/5030
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