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Mitochondrial import inner membrane translocase subunit TIM14 is an enzyme that in humans is encoded by the DNAJC19 gene on chromosome 3. [1]

28 relations: Apoptosis, ATPase, C-terminus, Cardiolipin, Cerebellar ataxia, Chaperone (protein), Dilated cardiomyopathy, Electrocardiography, Enzyme, Failure to thrive, Gene, Homology (biology), HSPA9, Microcytic anemia, Mitochondrial matrix, Mitochondrion, Mitophagy, Morphogenesis, N-terminus, PAM16, PHB2, Phospholipid, Prohibitin, QT interval, TIMM23, TIMM44, Transmembrane protein, 3-Methylglutaconic acid.

Apoptosis

Apoptosis (from Ancient Greek ἀπό apo, "by, from, of, since, than" and πτῶσις ptōsis, "fall") is the process of programmed cell death that may occur in multicellular organisms.

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ATPase

ATPases (adenylpyrophosphatase, ATP monophosphatase, triphosphatase, SV40 T-antigen, adenosine 5'-triphosphatase, ATP hydrolase, complex V (mitochondrial electron transport), (Ca2+ + Mg2+)-ATPase, HCO3−-ATPase, adenosine triphosphatase) are a class of enzymes that catalyze the decomposition of ATP into ADP and a free phosphate ion.

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C-terminus

The C-terminus (also known as the carboxyl-terminus, carboxy-terminus, C-terminal tail, C-terminal end, or COOH-terminus) is the end of an amino acid chain (protein or polypeptide), terminated by a free carboxyl group (-COOH).

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Cardiolipin

Cardiolipin (IUPAC name "1,3-bis(sn-3’-phosphatidyl)-sn-glycerol") is an important component of the inner mitochondrial membrane, where it constitutes about 20% of the total lipid composition.

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Cerebellar ataxia

Cerebellar ataxia is a form of ataxia originating in the cerebellum.

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Chaperone (protein)

In molecular biology, molecular chaperones are proteins that assist the covalent folding or unfolding and the assembly or disassembly of other macromolecular structures.

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Dilated cardiomyopathy

Not to be confused with hypertrophic cardiomyopathy or any other cardiomyopathy.

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Electrocardiography

Electrocardiography (ECG or EKG*) is the process of recording the electrical activity of the heart over a period of time using electrodes placed on a patient's body.

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Enzyme

Enzymes are macromolecular biological catalysts.

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Failure to thrive

Failure to thrive (FTT), more recently known as faltering weight or weight faltering, is a term used in pediatric, adult as well as veterinary medicine (where it is also referred to as ill thrift), to indicate insufficient weight gain or inappropriate weight loss.

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Gene

A gene is a locus (or region) of DNA that encodes a functional RNA or protein product, and is the molecular unit of heredity.

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Homology (biology)

In the context of biology, homology is the existence of shared ancestry between a pair of structures, or genes, in different species.

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HSPA9

Stress-70 protein, mitochondrial is a protein that in humans is encoded by the HSPA9 gene.

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Microcytic anemia

Microcytic anaemia is any of several types of anemia characterized by small red blood cells (called microcytes).

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Mitochondrial matrix

In the mitochondrion, the matrix contains soluble enzymes that catalyze the oxidation of pyruvate and other small organic molecules.

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Mitochondrion

The mitochondrion (plural mitochondria) is a double membrane-bound organelle found in most eukaryotic cells.

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Mitophagy

Mitophagy is the selective degradation of mitochondria by autophagy.

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Morphogenesis

Morphogenesis (from the Greek morphê shape and genesis creation, literally, "beginning of the shape") is the biological process that causes an organism to develop its shape.

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N-terminus

The N-terminus (also known as the amino-terminus, NH2-terminus, N-terminal end or amine-terminus) refers to the start of a protein or polypeptide terminated by an amino acid with a free amine group (-NH2).

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PAM16

Mitochondrial import inner membrane translocase subunit TIM16 also known as presequence translocated-associated motor subunit PAM16 is a protein that in humans is encoded by the PAM16 gene.

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PHB2

Prohibitin-2 is a protein that in humans is encoded by the PHB2 gene.

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Phospholipid

Phospholipids are a class of lipids that are a major component of all cell membranes.

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Prohibitin

Prohibitin, also known as PHB, is a protein that in humans is encoded by the PHB gene.

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QT interval

In cardiology, the QT interval is a measure of the time between the start of the Q wave and the end of the T wave in the heart's electrical cycle.

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TIMM23

Mitochondrial import inner membrane translocase subunit Tim23 is an enzyme that in humans is encoded by the TIMM23 gene.

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TIMM44

Mitochondrial import inner membrane translocase subunit TIM44 is an enzyme that in humans is encoded by the TIMM44 gene.

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Transmembrane protein

A transmembrane protein (TP) is a type of membrane protein spanning the entirety of the biological membrane to which it is permanently attached.

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3-Methylglutaconic acid

3-Methylglutaconic acid is a glutarate which builds up in the urine in 3-methylglutaconic aciduria or 3-hydroxy-3-methylglutaric aciduria.

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Redirects here:

DCMA syndrome, DNAJC19 (gene).

References

[1] https://en.wikipedia.org/wiki/DNAJC19

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