| ID | Sequence | Length | GC content |
|---|---|---|---|
| CGUUUCCGGUUGGCUCCGGUUGCAGAGUUGAGUGUCCUGAGAGGUCAGA… | 516 nt | 0.4070 | |
| CGUUUCCGGUUGGCUCCGGUUGCAGAGUUGAGUGUCCUGAGAGGUCAGA… | 493 nt | 0.4077 |
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]
A study in humans identified the NDUFB3 as one of the top ten most central mitochondrial genes via protein-protein interaction network analysis in sepsis patients [Li et al. DOI:10.1186/s12920-024-01891-x].