| Gene Name | TMEM126B |
|
| Specie | Homo sapiens | |
| Full Name | transmembrane protein 126B | |
| Also known as | HT007|MC1DN29 | |
| Coordinate | chr11:85628573-85636540 | |
| Strand | + | |
| Gene summary | This gene encodes a mitochondrial transmembrane protein which is a component of the mitochondrial complex I assembly complex. The encoded protein serves as an assembly factor that is required for formation of the membrane arm of the complex. It interacts with NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 13. Naturally occurring mutations in this gene are associated with isolated complex I deficiency. A pseudogene of this gene has been defined on chromosome 9. [provided by RefSeq, Apr 2017] |
| Retroname | Coord | Strand | Genomic Region | ENSG | |
|---|---|---|---|---|---|
| TMEM126BP1 | chr9:73871424-73871617 | - |
Intergenic |
ENSG00000223368 | UCSC |
| >NM_001256547.2 |
| TCCCCGCCCACCGGCAAGTCACATGAGCCACCAAAATGGTGGTGTTCGGGTATGAGGCTGGGACTAAGCCAAGGGATTCAGGTGTGGTGCCGGTGGGAACTGAGGAAGCGCCCAAGGACACAAAATATATATCAAATGGCGACATTTGGAACAACAGCTGGTTTCTCTGGAATATTCTCAAACTTCCTGTTCAGACGCTGCTTCAAGGTTAAACATGATGCTTTGAAGACATATGCATCATTGGCTACACTTCCATTTTTGTCTACTGTTGTTACTGACAAGCTTTTTGTAATTGATGCTTTGTATTCAGATAATATAAGCAAGGAAAACTGTGTTTTCAGAAGCTCACTGATTGGCATAGTTTGTGGTGTTTTCTATCCCAGTTCTTTGGCTTTTACTAAAAATGGACGCCTGGCAACCAAGTATCATACCGTTCCACTGCCACCAAAAGGAAGGGTTTTAATCCATTGGATGACGCTTTGTCAAACACAAATGAAATTAATGGCGATTCCTCTAGTCTTTCAGATTATGTTTGGAATATTAAATGGTCTATACCATTATGCAGTATTTGAAGAGACACTTGAGAAAACTATACATGAAGAGTAACCAAAAAAATGAATGGTTGCTAACTTAGCAAAATGAAGTTTCTATAAAGAGGACTCAGGCATTGCTGAAAGAGTTAAAAGTAACTGTGAACAAATAATTTGTTCTGTGCCTTTTGCCTGGTATATAGCAAATACTCAAAAAGTATTCAATAATTCAATCAATAAATATAAGTTTCATCTTACACGTAAGATACAGGTCTTATCTCCTGATGGTGTGTCCATTTTGCCTGGTATATAACAGATAATAAATATCCAGTGTCAATAAATGTAACAATAAAAGTTTCATCTTTCCTCTTTGTATGTGGAAATGGG |