QuickView for SLC22A5;jsessionid=E86C91F9B8BE4DFDCD9CAC774BB01A94;jsessionid=99B012D2CF49229655EA638EE1C2B073;jsessionid=964F851AA22FA60B56C96D92B4FA84EC (gene)

Summary
General Info

Body Atlas

Most Correlated Tissues

Kidney cortex
Colon mucosa
Ileum mucosa
Kidney medulla
Kidney

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Disease Atlas

Most Correlated Diseases

Renal carnitine transport defect
Carnitine deficiency
Multiple organ failure
11p partial monosomy syndrome
Eating / feeding / drinking finding

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Pharmaco Atlas

Most Correlated Compounds

Carnitine
ciprofibrate
alpha-naphthoflavone
benziodarone
Nafenopin

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Knockdown Atlas

Most Correlated Gene Perturbations

MCF2L
CLOCK
RPA2
PPARA
DEL22Q11.2

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Curated Studies

Most Correlated Studies

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Literature

Most Relevant Literature

Efficient Oral Delivery of Poorly Water-Soluble Drugs Using Carnitine/Organic Cation Transporter 2-M…
Slc22a5 haploinsufficiency does not aggravate the phenotype of the long-chain acyl-CoA dehydrogenase…
Carnitine and γ-Butyrobetaine Stimulate Elimination of Meldonium due to Competition for OCTN2-mediat…
Evaluation of the gene encoding carnitine transporter (OCTN2/SLC22A5) expression in human breast can…
The activity and surface presence of organic cation/carnitine transporter OCTN2 (SLC22A5) in breast …

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Clinical Trials

Most Relevant Clinical Trials

There were no clinical trials for SLC22A5;jsessionid=E86C91F9B8BE4DFDCD9CAC774BB01A94;jsessionid=99B012D2CF49229655EA638EE1C2B073;jsessionid=964F851AA22FA60B56C96D92B4FA84EC

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