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Ovarian Kaleidoscope Database (OKdb)

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MTND5 OKDB#: 5834
 Symbols: ND5 Species: human
 Synonyms: MTND5  Locus:


For retrieval of Nucleotide and Amino Acid sequences please go to: OMIM Entrez Gene
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General Comment non-nuclear////////////////Heteroplasmic mutations in the MTND5 gene can result in several different mitochondrial disorders, including Leber hereditary optic neuropathy (LHON; 535000), MELAS syndrome (540000), Leigh syndrome (256000), and complex I deficiency (252010).

General function Enzyme
Comment
Cellular localization Mitochondrial
Comment
Ovarian function
Comment
Expression regulated by
Comment
Ovarian localization Oocyte
Comment
Follicle stages
Comment
Phenotypes
Mutations 0 mutations
Genomic Region show genomic region
Phenotypes and GWAS show phenotypes and GWAS
Links
OMIM (Online Mendelian Inheritance in Man: an excellent source of general gene description and genetic information.)
OMIM \ Animal Model
KEGG Pathways
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created: Aug. 4, 2020, 1:44 p.m. by: system   email:
home page:
last update: Aug. 4, 2020, 1:46 p.m. by: hsueh    email:



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