| Gene Name | TMEM126A |
|
| Specie | Homo sapiens | |
| Full Name | transmembrane protein 126A | |
| Also known as | OPA7 | |
| Coordinate | chr11:85647967-85656542 | |
| Strand | + | |
| Gene summary | The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011] |
| Retroname | Coord | Strand | Genomic Region | ENSG | |
|---|---|---|---|---|---|
| TMEM126AP2 | chr15:65025969-65026715 | + |
Intragenic |
ENSG00000270218 | UCSC |
| TMEM126AP1 | chr5:38763812-38764227 | - |
Intergenic |
ENSG00000248577 | UCSC |
| >NM_032273.4 |
| ACGCCGCGTCACGAGTCAGCCAAAGATGGCTGCGCCCAGGTAATTTGAGCAAAGGCCACAGTGAACTCCGGCGTGGCTGAGGAAGGAGGAGGCACCCACAGGCTGCTGGGAGGAGAGCATAAGGCTCAAAATGGAAAATCATAAATCCAATAATAAGGAAAACATAACAATTGTTGATATATCCAGAAAAATTAACCAGCTTCCAGAAGCAGAAAGGAATCTACTTGAAAATGGATCGGTTTATGTTGGATTAAATGCTGCTCTTTGTGGCCTCATAGCAAACAGTCTTTTTCGACGCATCTTGAATGTGACAAAGGCTCGCATAGCTGCTGGCTTACCAATGGCAGGGATACCTTTTCTTACAACAGACTTAACTTACAGATGTTTTGTAAGTTTTCCTTTGAATACAGGTGATTTGGATTGTGAAACCTGTACCATAACACGGAGTGGACTGACTGGTCTTGTTATTGGTGGTCTATACCCTGTTTTCTTGGCTATACCTGTAAATGGTGGTCTAGCAGCCAGGTATCAATCAGCTCTGTTACCACACAAAGGGAACATCTTAAGTTACTGGATTAGAACTTCTAAGCCTGTCTTTAGAAAGATGTTATTTCCTATTTTGCTCCAGACTATGTTTTCAGCATACCTTGGGTCTGAACAATATAAACTACTTATAAAGGCCCTTCAGTTATCTGAACCTGGCAAAGAAATTCACTGATTTTAAACAAATATGTAAACAAAAATAAAATGGTAAAAACA |