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- Table of Contents
Facts about Required for meiotic nuclear division protein 1 homolog.
Human | |
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Gene Name: | RMND1 |
Uniprot: | Q9NWS8 |
Entrez: | 55005 |
Belongs to: |
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RMD1/sif2 family |
bA351K16; bA351K16.3; C6orf96; chromosome 6 open reading frame 96; FLJ20627; MGC117362; MGC149570; MGC88260; required for meiotic nuclear division 1 homolog (S. cerevisiae); required for meiotic nuclear division protein 1 homolog; RMD1
Mass (kDA):
51.604 kDA
Human | |
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Location: | 6q25.1 |
Sequence: | 6; NC_000006.12 (151404548..151452181, complement) |
Mitochondrion. May be localized in mitochondrial RNA granules (PubMed:25604853).
PMID: 23022099 by Garcia-Diaz B., et al. Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation.
PMID: 25604853 by Janer A., et al. RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement.