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Gene: MT-ND5 (mitochondrially encoded NADH dehydrogenase 5) Homo sapiens
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Symbol: MT-ND5
Name: mitochondrially encoded NADH dehydrogenase 5
Description: Predicted to be involved in mitochondrial electron transport, NADH to ubiquinone and mitochondrial respiratory chain complex I assembly. Localizes to the mitochondrial respiratory chain complex I. Implicated in Leber hereditary optic neuropathy; Leigh disease; and MELAS syndrome; INTERACTS WITH 3-isobutyl-1-methyl-7H-xanthine; atrazine; beauvericin.
Type: protein-coding
RefSeq Status: PROVISIONAL
Also known as: MTND5; NADH dehydrogenase subunit 5; NADH dehydrogenase, subunit 5 (complex I)
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38MT12,337 - 14,148 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37MT12,337 - 14,148 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36MT12,338 - 14,149 (+)NCBINCBI36hg18NCBI36
Cytogenetic MapMT NCBI


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Phenotype Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on MT-ND5
Alliance Gene
NCBI Gene
Ensembl Gene
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1347448
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-10-08
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.