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RMND1 产品

(Required For Meiotic Nuclear Division 1 Homolog (RMND1))

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The protein encoded by this gene belongs to the evolutionary conserved sif2 family of proteins that share the DUF155 domain in common. This protein is thought to be localized in the mitochondria and involved in mitochondrial translation. Mutations in this gene are associated with combined oxidative phosphorylation deficiency-11. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2012].

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Featured RMND1 Categories

RMND1 抗体

High quality antibodies with extensive validation data.

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Latest Publications for our RMND1 Products

Garcia-Diaz, Barros, Sanna-Cherchi, Emmanuele, Akman, Ferreiro-Barros, Horvath, Tadesse, El Gharaby, DiMauro, De Vivo, Shokr, Hirano, Quinzii: "Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation." in: American journal of human genetics, Vol. 91, Issue 4, pp. 729-36, (2012) (PubMed).

Synonyms and alternative names related to RMND1

required for meiotic nuclear division 1 homolog (RMND1), required for meiotic nuclear division 1 homolog (rmnd1), required for meiotic nuclear division 1 homolog (Rmnd1), 0610042C05Rik, AA408137, AI462664, AW536662, bA351K16, bA351K16.3, C6orf96, COXPD11, DKFZp469I1433, Iag-1, RGD1309546, RMD1, zgc:113022

Protein level used designations for RMND1

  • required for meiotic nuclear division 1 homolog (S. cerevisiae)
  • required for meiotic nuclear division protein 1 homolog
  • required for meiotic nuclear division protein 1 homolog-like
  • implantation-associated gene-1
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