OPA1 gene homepage
MSeqDR-LSDB: Mitochondrial Disease LSDB
General information |
Gene symbol |
OPA1 |
Gene name |
optic atrophy 1 (autosomal dominant) |
Chromosome |
3 |
Chromosomal band |
q28-q29 |
Imprinted |
Unknown |
Genomic reference |
NC_000003.11 |
Transcript reference |
NM_015560.2, NM_130831.2, NM_130832.2, NM_130833.2, NM_130834.2, NM_130835.2, NM_130836.2, NM_130837.2 |
Associated with diseases |
616896, DOA+, OPA1 |
Citation reference(s) |
- |
Curators (0) |
- |
Total number of public variants reported |
77 |
Unique public DNA variants reported |
64 |
Individuals with public variants |
0 |
Hidden variants |
0 |
Download all this gene's data |
Download all data |
Notes |
MSeqDR-LSDB |
Date created |
November 07, 2013 |
Active transcripts
Copyright & disclaimer |
Sources: GeneDX http://www.genedx.com ; NuclearMitome http://www.transgenomic.com ; MitoPhenome http://mitophenome.org ; MitoCarta http://www.broadinstitute.org/pubs/MitoCarta/ |
Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium
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