Matches in DBpedia 2014 for { <http://dbpedia.org/resource/SLC22A5> ?p ?o. }
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- SLC22A5 abstract "SLC22A5 is a membrane transport protein associated with primary carnitine deficiency.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.".
- SLC22A5 entrezgene "6584".
- SLC22A5 wikiPageExternalLink OCTN2_welcome.php.
- SLC22A5 wikiPageID "10744725".
- SLC22A5 wikiPageRevisionID "586585380".
- SLC22A5 hasPhotoCollection SLC22A5.
- SLC22A5 requireManualInspection "no".
- SLC22A5 summaryText "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 , an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy.".
- SLC22A5 updateCitations "yes".
- SLC22A5 updatePage "yes".
- SLC22A5 updateProteinBox "yes".
- SLC22A5 updateSummary "yes".
- SLC22A5 subject Category:Amphetamine.
- SLC22A5 subject Category:Solute_carrier_family.
- SLC22A5 type Biomolecule.
- SLC22A5 type Protein.
- SLC22A5 type BiologicalObject.
- SLC22A5 comment "SLC22A5 is a membrane transport protein associated with primary carnitine deficiency.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.".
- SLC22A5 label "SLC22A5".
- SLC22A5 sameAs m.02qnw41.
- SLC22A5 sameAs Q7390798.
- SLC22A5 sameAs Q7390798.
- SLC22A5 sameAs SLC22A5.
- SLC22A5 sameAs 118.
- SLC22A5 wasDerivedFrom SLC22A5?oldid=586585380.
- SLC22A5 isPrimaryTopicOf SLC22A5.