| Name |
|---|
NDUFA3P3 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 3 pseudogene 3 |
NDUFB11P1 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 11, pseudogene 1 |
NDUFA3P1 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 3 pseudogene 1 |
NDUFB1P2 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 1 pseudogene 2 |
NDUFB4P1 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 4, 15kDa pseudogene 1 |
LOC100884169 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 12 pseudogene |
LOC100128711 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 10, 22kDa pseudogene |
LOC100128596 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa pseudogene |
NDUFA11 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 11, 14.7kDa This gene encodes a subunit of the membrane-bound mitochondrial complex I. Complex I is composed of numerous subunits and functions as the NADH-ubiquinol reductase of the mitochondrial electron transport chain. Mutations in this gene are associated with severe mitochondrial complex I deficiency. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2010] |
NDUFA12 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 12 This gene encodes a protein which is part of mitochondrial complex 1, part of the oxidative phosphorylation system in mitochondria. Complex 1 transfers electrons to ubiquinone from NADH which establishes a proton gradient for the generation of ATP. Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2012] |
NDUFA13 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13 This gene encodes a subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), which functions in the transfer of electrons from NADH to the respiratory chain. The protein is required for complex I assembly and electron transfer activity. The protein binds the signal transducers and activators of transcription 3 (STAT3) transcription factor, and can function as a tumor suppressor. The human protein purified from mitochondria migrates at approximately 16 kDa. Transcripts originating from an upstream promoter and capable of expressing a protein with a longer N-terminus have been found, but their biological validity has not been determined. [provided by RefSeq, Oct 2009] |
LOC100505788 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 4, 9kDa pseudogene |
NDUFB8P1 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 8, pseudogene 1 |
NDUFB8P3 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 8, pseudogene 3 |
LOC100129370 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa pseudogene |
LOC102724035 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 pseudogene |
NDUFB4P2 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 4, 15kDa pseudogene 2 |
NDUFB3P5 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 3, 12kDa pseudogene 5 |
NDUFB9 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa The protein encoded by this gene is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015] |
NDUFB8 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 8, 19kDa Predicted to enable NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial respiratory chain complex I assembly. Located in mitochondrion. Part of mitochondrial inner membrane and respiratory chain complex I. Implicated in nuclear type mitochondrial complex I deficiency 32. Biomarker of Alzheimer's disease and Parkinson's disease. [provided by Alliance of Genome Resources, Mar 2025] |
NDUFB7 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 7, 18kDa The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is composed of 45 different subunits. It is located at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. [provided by RefSeq, Jul 2008] |
NDUFB6 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 6, 17kDa The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is composed of 45 different subunits. It locates at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Alternative splicing occurs at this locus and three transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jan 2011] |
NDUFB5 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 5, 16kDa The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is composed of 45 different subunits. It locates at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011] |
NDUFB4 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 4, 15kDa This gene encodes a non-catalytic subunit of the multisubunit NADH:ubiquinone oxidoreductase, the first enzyme complex in the mitochondrial electron transport chain (complex I). Mammalian complex I is composed of 45 different subunits and transfers electrons from NADH to ubiquinone. [provided by RefSeq, Dec 2009] |
NDUFB3 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 3, 12kDa This gene encodes an accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which is the first enzyme in the electron transport chain of mitochondria. This protein localizes to the inner membrane of the mitochondrion as a single-pass membrane protein. Mutations in this gene contribute to mitochondrial complex 1 deficiency. Alternative splicing results in multiple transcript variants encoding the same protein. Humans have multiple pseudogenes of this gene. [provided by RefSeq, Mar 2012] |
NDUFB2 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 2, 8kDa The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is composed of 45 different subunits. This protein has NADH dehydrogenase activity and oxidoreductase activity. It plays a important role in transfering electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Hydropathy analysis revealed that this subunit and 4 other subunits have an overall hydrophilic pattern, even though they are found within the hydrophobic protein (HP) fraction of complex I. [provided by RefSeq, Jul 2008] |
NDUFB1 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 1, 7kDa Predicted to enable NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial respiratory chain complex I assembly. Located in mitochondrion and nuclear speck. Part of mitochondrial inner membrane and respiratory chain complex I. [provided by Alliance of Genome Resources, Mar 2025] |
NDUFB3P2 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 3, 12kDa pseudogene 2 |
NDUFB3P3 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 3, 12kDa pseudogene 3 |
NDUFB3P1 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 3, 12kDa pseudogene 1 |
NDUFB3P4 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 3, 12kDa pseudogene 4 |
NDUFA6 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 6, 14kDa This gene encodes a member of the LYR family of proteins that contain a highly conserved tripeptide (LYR) motif near the N-terminus. The encoded protein is an accessory subunit of NADH: ubiquinone oxidorerductase (Complex I), which is the largest enzyme of the mitochondrial membrane respiratory chain. Complex I functions in electron transfer from NADH to the respiratory chain. [provided by RefSeq, Oct 2016] |
NDUFA7 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 7, 14.5kDa This gene encodes a subunit of NADH:ubiquinone oxidoreductase (complex I), which is a multiprotein complex located in the inner mitochondrial membrane. Complex I functions in the transfer of electrons from NADH to the respiratory chain. [provided by RefSeq, Mar 2011] |
NDUFA5 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 This nuclear gene encodes a conserved protein that comprises the B13 subunit of complex I of the mitochondrial respiratory chain. The encoded protein localizes to the inner mitochondrial membrane, where it is thought to aid in the transfer of electrons from NADH to ubiquinone. Alternative splicing results in multiple transcript variants. There are numerous pseudogenes of this gene on chromosomes 1, 3, 6, 8, 9, 11, 12, and 16. [provided by RefSeq, Apr 2014] |
NDUFA2 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 2, 8kDa The encoded protein is a subunit of the hydrophobic protein fraction of the NADH:ubiquinone oxidoreductase (complex 1), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane, and may be involved in regulating complex I activity or its assembly via assistance in redox processes. Mutations in this gene are associated with Leigh syndrome, an early-onset progressive neurodegenerative disorder. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010] |
NDUFA3 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 3, 9kDa Predicted to enable NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial respiratory chain complex I assembly. Located in mitochondrion. Part of mitochondrial inner membrane and respiratory chain complex I. [provided by Alliance of Genome Resources, Mar 2025] |
NDUFA1 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 1, 7.5kDa The human NDUFA1 gene codes for an essential component of complex I of the respiratory chain, which transfers electrons from NADH to ubiquinone. It has been noted that the N-terminal hydrophobic domain has the potential to be folded into an alpha-helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular subunits of complex I. The highly conserved two-domain structure suggests that this feature is critical for the protein function and might act as an anchor for the NADH:ubiquinone oxidoreductase complex at the inner mitochondrial membrane. However, the NDUFA1 peptide is one of about 31 components of the `hydrophobic protein` (HP) fraction of complex I which is involved in proton translocation. Thus the NDUFA1 peptide may also participate in that function. [provided by RefSeq, Jul 2008] |
NDUFA8 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 8, 19kDa The protein encoded by this gene belongs to the complex I 19 kDa subunit family. Mammalian complex I is composed of 45 different subunits. This protein has NADH dehydrogenase activity and oxidoreductase activity. It plays an important role in transfering electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015] |
NDUFA9 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 9, 39kDa The encoded protein is a subunit of the hydrophobic protein fraction of the NADH:ubiquinone oxidoreductase (complex I), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane. A pseudogene has been identified on chromosome 12. [provided by RefSeq, May 2010] |
LOC102724070 GeneNADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 5 pseudogene |
LOC100422431 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 5, 16kDa pseudogene |
NDUFA5P5 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 pseudogene 5 |
NDUFA5P4 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 pseudogene 4 |
NDUFA5P6 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 pseudogene 6 |
NDUFA5P1 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 pseudogene 1 |
NDUFA5P3 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 pseudogene 3 |
NDUFA9P1 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 9, pseudogene 1 |
NDUFA5P12 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 pseudogene 12 |
LOC102724853 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 pseudogene |
NDUFA5P9 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 pseudogene 9 |
NDUFA4P1 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 4, 9kDa, pseudogene 1 |
NDUFA4P2 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 4, 9kDa, pseudogene 2 |
NDUFA4L2 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 4-like 2 Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100288420 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 4, 15kDa pseudogene |
NDUFA10 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 10, 42kDa The protein encoded by this gene is a component of 42 kDa complex I, the first enzyme complex in the electron transport chain of mitochondria. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. A mutation in this gene was found in an individual with Leigh syndrome. [provided by RefSeq, Apr 2016] |
LOC100288337 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 5, 16kDa pseudogene |
LOC103091863 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 pseudogene |
NDUFC1 GeneNADH dehydrogenase (ubiquinone) 1, subcomplex unknown, 1, 6kDa The encoded protein is a subunit of the NADH:ubiquinone oxidoreductase (complex I), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010] |
NDUFC2 GeneNADH dehydrogenase (ubiquinone) 1, subcomplex unknown, 2, 14.5kDa Predicted to enable NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial respiratory chain complex I assembly. Located in mitochondrion. Part of mitochondrial inner membrane and respiratory chain complex I. Implicated in nuclear type mitochondrial complex I deficiency. [provided by Alliance of Genome Resources, Mar 2025] |
NDUFAB1 GeneNADH dehydrogenase (ubiquinone) 1, alpha/beta subcomplex, 1, 8kDa Enables mitochondrial large ribosomal subunit binding activity. Involved in [2Fe-2S] cluster assembly; mitochondrial respiratory chain complex I assembly; and protein lipoylation. Located in mitochondrion and nucleoplasm. Part of mitochondrial [2Fe-2S] assembly complex; mitochondrial inner membrane; and respiratory chain complex I. [provided by Alliance of Genome Resources, Mar 2025] |
NDUFA12P1 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 12 pseudogene 1 |
NDUFB8P2 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 8, pseudogene 2 |
NDUFB1P1 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 1 pseudogene 1 |
NDUFB11 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 11, 17.3kDa The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is located at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to ubiquinone. Mutations in the human gene are associated with linear skin defects with multiple congenital anomalies 3 and mitochondrial complex I deficiency. [provided by RefSeq, Dec 2016] |
NDUFB10 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 10, 22kDa Predicted to enable NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial respiratory chain complex I assembly. Located in mitochondrion. Part of mitochondrial inner membrane and respiratory chain complex I. Implicated in nuclear type mitochondrial complex I deficiency 35. [provided by Alliance of Genome Resources, Mar 2025] |
LOC102724866 GeneNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 pseudogene |
LOC402175 GeneNADH dehydrogenase (ubiquinone) 1 beta subcomplex, 4, 15kDa pseudogene |