OCTN2/SLC22A5 Products

Lysates
OCTN2/SLC22A5 Overexpression ...
OCTN2/SLC22A5 Overexpression Lysat...
NBL1-16037
Applications: WB
Proteins
OCTN2/SLC22A5 Recombinant Pro ...
OCTN2/SLC22A5 Recombinant Protein
H00006584-P01
Species: Hu
Applications: WB, ELISA, PA
OCTN2/SLC22A5 Partial Recombi ...
OCTN2/SLC22A5 Partial Recombinant ...
H00006584-Q01
Species: Hu
Applications: WB, ELISA, PA
RNAi
OCTN2/SLC22A5 RNAi
OCTN2/SLC22A5 RNAi
H00006584-R01
Species: Hu

Description

Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy. [provided by RefSeq]

Bioinformatics

Entrez Human
Uniprot Human
Human
Human
Product By Gene ID 6584
Alternate Names
  • FLJ46769
  • solute carrier family 22 member 5
  • CDSP
  • solute carrier family 22 (organic cation transporter), member 5
  • SCD
  • organic cation transporter 5
  • Organic cation/carnitine transporter 2
  • organic cation transporter 2
  • High-affinity sodium-dependent carnitine cotransporter
  • OCTN2high-affinity sodium dependent carnitine cotransporter
  • OCTN2VT
  • solute carrier family 22 (organic cation/carnitine transporter), member 5

Bioinformatics Tool for OCTN2/SLC22A5

Discover related pathways, diseases and genes to OCTN2/SLC22A5. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.
 
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