RMND1

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]

Description

Required for meiotic nuclear division 1 homolog

Tissue specificity

Low tissue specificity

Subcell location

Mitochondria

Predicted location

Intracellular, Membrane

Protein family

Disease related genes
Human disease related genes
Mapped to neXtProt
Mapped to UniProt SWISS-PROT
Predicted intracellular proteins
Predicted membrane proteins
Protein evidence (Ezkurdia et al 2014)
Protein evidence (Kim et al 2014)

Chromosome

6 (151404762 - 151452158)

Ensembl ID

ENSG00000155906  (ver. 103.38)

Orthologs

Mouse Rmnd1: ENSMUSG00000019763

UniProt

Q9NWS8

neXtProt

NX_Q9NWS8

Human splice variants
Mouse splice variants

Protein structure