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Carnitine palmitoyltransferase II information


CPT2
Identifiers
AliasesCPT2, CPT1, CPTASE, IIAE4, carnitine palmitoyltransferase 2
External IDsOMIM: 600650; MGI: 109176; HomoloGene: 77; GeneCards: CPT2; OMA:CPT2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000098
NM_001330589

NM_009949

RefSeq (protein)

NP_000089
NP_001317518

NP_034079

Location (UCSC)Chr 1: 53.2 – 53.21 MbChr 4: 107.76 – 107.78 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Carnitine O-palmitoyltransferase 2, mitochondrial is an enzyme that in humans is encoded by the CPT2 gene.[5][6]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000157184 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028607 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Minoletti F, Colombo I, Martin AL, Di Donato S, Taroni F, Finocchiaro G, Pandolfo M (Sep 1992). "Localization of the human gene for carnitine palmitoyltransferase to 1p13-p11 by nonradioactive in situ hybridization". Genomics. 13 (4): 1372–1374. doi:10.1016/0888-7543(92)90076-5. PMID 1339389. (Retracted)
  6. ^ "Entrez Gene: CPT2 carnitine palmitoyltransferase II".

and 24 Related for: Carnitine palmitoyltransferase II information

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Carnitine palmitoyltransferase II

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Carnitine O-palmitoyltransferase 2, mitochondrial is an enzyme that in humans is encoded by the CPT2 gene. Carnitine palmitoyltransferase II precursor...

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Carnitine palmitoyltransferase II deficiency

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Carnitine palmitoyltransferase II deficiency, sometimes shortened to CPT-II or CPT2, is an autosomal recessively inherited genetic metabolic disorder...

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Carnitine palmitoyltransferase I

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Carnitine palmitoyltransferase I (CPT1) also known as carnitine acyltransferase I, CPTI, CAT1, CoA:carnitine acyl transferase (CCAT), or palmitoylCoA transferase...

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Carnitine palmitoyltransferase I deficiency

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Carnitine palmitoyltransferase I deficiency is a rare metabolic disorder that prevents the body from converting certain fats called long-chain fatty acids(LCFA)...

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Carnitine

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acetylcarnitine ester and being transported by carnitine palmitoyltransferase I and carnitine palmitoyltransferase II. Carnitine also plays a role in stabilizing acetyl-CoA...

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Inborn error of lipid metabolism

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Carnitine palmitoyltransferase I deficiency (CPT) - Carnitine palmitoyltransferase I Carnitine palmitoyltransferase II deficiency (CPT) - Carnitine palmitoyltransferase...

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Myalgia

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Polyarteritis nodosa Devic's disease Morphea Sarcoidosis Carnitine palmitoyltransferase II deficiency Conn's syndrome Adrenal insufficiency Hyperthyroidism...

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Fasciculation

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clinicians are overrepresented in study samples. Blepharospasm Carnitine palmitoyltransferase II deficiency Myokymia Fibrillation Myoclonus Seizure and convulsion...

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Hardgainer

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processes in the body: Acid maltase deficiency Carnitine deficiency Carnitine palmitoyltransferase II deficiency Debrancher Enzyme Deficiency Lactate...

Word Count : 383

Chromosome 1

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COL16A1 (1p35) COL11A1: collagen, type XI, alpha 1 CPT2: carnitine palmitoyltransferase II CRYZ: Crystallin zeta CSDE1: Cold shock domain containing...

Word Count : 3284

CAT II

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CAT II may refer to: Instrument landing system#ILS categories Chloramphenicol O-acetyltransferase II, an enzyme Carnitine O-palmitoyltransferase II, another...

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Beta oxidation

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acyl-CoA by carnitine palmitoyltransferase II, located on the interior face of the inner mitochondrial membrane. The liberated carnitine is shuttled back to...

Word Count : 3362

Meldonium

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protein called carnitine-acylcarnitine translocase. Once inside, carnitine is liberated (catalysed by the enzyme carnitine palmitoyltransferase II) and transported...

Word Count : 4893

Triheptanoin

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metabolic diseases, such as pyruvate carboxylase deficiency and carnitine palmitoyltransferase II deficiency. It also appears to increase the efficacy of the...

Word Count : 969

Myokymia

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-kŷmia – "something swollen" or -kŷmos – "wave". Blepharospasm Carnitine palmitoyltransferase II deficiency Fasciculation Myoclonic jerk (myoclonus) Walton...

Word Count : 447

Hyperammonemia

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Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Carnitine palmitoyltransferase II deficiency Transient hyperammonemia of the newborn, specifically...

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Myoglobinuria

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include: McArdle's disease Phosphofructokinase deficiency Carnitine palmitoyltransferase II deficiency Malignant hyperthermia Polymyositis Lactate dehydrogenase...

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List of neuromuscular disorders

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Phosphoglycerate kinase deficiency Carnitine palmitoyltransferase I deficiency Carnitine palmitoyltransferase II deficiency Medium-chain acyl-coenzyme...

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Glycogen storage disease type V

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This can help distinguish McArdle's syndrome from carnitine palmitoyltransferase II deficiency (CPT-II), a lipid-based metabolic disorder which prevents...

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Transferase

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rely on controlling the diet of the patient. Carnitine palmitoyltransferase II deficiency (also known as CPT-II deficiency) leads to an excess long chain...

Word Count : 6229

CPT2

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CPT2 may refer to: Carnitine palmitoyltransferase II, an important metabolic enzyme. Carnitine palmitoyltransferase II deficiency, a condition that prevents...

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Fatty acid metabolism

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acyl-CoA by carnitine palmitoyltransferase II, located on the interior face of the inner mitochondrial membrane. The liberated carnitine is shuttled back...

Word Count : 5569

Fatty acid degradation

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translocase Acyl carnitine (such as Palmitoylcarnitine) is converted to acyl CoA by carnitine acyltransferase (palmitoyltransferase) II located on the inner...

Word Count : 685

Etomoxir

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dextrorotatory (R)-(+)- enantiomer, is an irreversible inhibitor of carnitine palmitoyltransferase-1 (CPT-1; EC 2.3.1.21) on the inner face of the outer mitochondrial...

Word Count : 1783

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