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carnitine palmitoyltransferase 2
The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders. [provided by RefSeq]
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| Cecum |
100
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| Epidermis |
92
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| Skeletal muscle tiss… |
88
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| Colon |
86
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| Adipose tissue |
86
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| Tongue |
84
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|---|---|---|---|
| Perhexilene |
100
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| Levocarnitine |
100
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| Kanamycin |
89
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| Angiotensin Ii |
87
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| Candesartan |
85
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| Roxarsone |
84
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|---|---|---|---|
| Carnitine palmitoylt… |
100
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| Myopathy |
99
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| Starvation |
73
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| Coccidiosis |
48
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| Dehydration |
47
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| Caloric restriction … |
43
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Individual Studies |
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Authors: Paul J Isackson, Michael J Bennett, Uta Lichter-Konecki, Mary Willis, William L Nyhan, V Reid Sutton, Ingrid Tein, Georgirene D Vladutiu
Molecular genetics and metabolism 2008 AugAuthors: Laure Thuillier, Hidayeth Rostane, Veronique Droin, France Demaugre, Michèle Brivet, Noman Kadhom, Carina Prip-Buus, Stéphanie Gobin, Jean-Marie Saudubray, Jean-Paul Bonnefont
Human mutation 2003 MayThought leaders and organizations working on research involving CPT2.
conditions: Carnitine Palmitoyl Transferase 2 Deficiency
interventions: bezafibrate (drug)
conditions: Inborn Errors of Metabolism
interventions: Oil special 107 and MYGLIOL 810