39S ribosomal protein L22, mitochondrial is a protein that in humans is encoded by the MRPL22 gene.
39S ribosomal protein L30, mitochondrial is a protein that in humans is encoded by the MRPL30 gene.
Tryptophanyl-tRNA synthetase, mitochondrial is an enzyme that in humans is encoded by the WARS2 gene.
Protein MTO1 homolog, mitochondrial is a protein that in humans is encoded by the MTO1 gene.
28S ribosomal protein S16, mitochondrial is a protein that in humans is encoded by the MRPS16 gene.
28S ribosomal protein S26, mitochondrial is a protein that in humans is encoded by the MRPS26 gene.
39S ribosomal protein L40, mitochondrial is a protein that in humans is encoded by the MRPL40 gene.
39S ribosomal protein L24, mitochondrial is a protein that in humans is encoded by the MRPL24 gene.
39S ribosomal protein L37, mitochondrial is a protein that in humans is encoded by the MRPL37 gene.
39S ribosomal protein L23, mitochondrial is a protein that in humans is encoded by the MRPL23 gene.
28S ribosomal protein S35, mitochondrial is a protein that in humans is encoded by the MRPS35 gene.
39S ribosomal protein L10, mitochondrial is a protein that in humans is encoded by the MRPL10 gene.
Alanyl—tRNA synthetase, mitochondrial, also known as alanine—tRNA ligase (AlaRS) or alanyl—tRNA synthetase 2 (AARS2), is an enzyme that in humans is encoded by the AARS2 gene.
NOP2/Sun domain family, member 2 is a protein that in humans is encoded by the NSUN2 gene. Alternatively spliced transcript variants encoding different isoforms have been noted for the gene.
Mitochondrial ribosomal protein L3 is a protein that in humans is encoded by the MRPL3 gene.
Dehydrogenase E1 and transketolase domain containing 1 is a protein that in humans is encoded by the DHTKD1 gene. This gene encodes a component of a mitochondrial 2-oxoglutarate-dehydrogenase-complex-like protein involved in the degradation pathways of several amino acids, including lysine. Mutations in this gene are associated with 2-aminoadipic 2-oxoadipic aciduria and Charcot-Marie-Tooth Disease Type 2Q.
Solute carrier family 25 member 22 is a protein that in humans is encoded by the SLC25A22 gene. This gene encodes a mitochondrial glutamate carrier. Mutations in this gene are associated with early infantile epileptic encephalopathy. Expression of this gene is increased in colorectal tumor cells.
Ribonuclease H2 subunit C is a protein that in humans is encoded by the RNASEH2C gene. RNase H2 is composed of a single catalytic subunit (A) and two non-catalytic subunits, and degrades the RNA of RNA:DNA hybrids.
Mitochondrial ribosomal protein L13 is a protein that in humans is encoded by the MRPL13 gene.
Valyl-tRNA synthetase 2, mitochondrial is a protein that in humans is encoded by the VARS2 gene.
