Wikidata entity: Q18030277
| P1057 | chromosome | ... | Q668633 (human chromosome 3) | human chromosome 3 |
| P4196 | cytogenetic location | String | 3q29 | ??? |
| P688 | encodes | ... | Q21106682 (OPA1 mitochondrial dynamin like GTPase) | OPA1 mitochondrial dynamin like GTPase |
| P2888 | exact match | Url | None | ??? |
| P5572 | expressed in | ... | Q158716 (rectum) | rectum |
| P5572 | expressed in | ... | Q66509944 (secondary oocyte) | secondary oocyte |
| P5572 | expressed in | ... | Q66558397 (lateral nuclear group of thalamus) | lateral nuclear group of thalamus |
| P5572 | expressed in | ... | Q107244 (monocyte) | monocyte |
| P5572 | expressed in | ... | Q1308310 (right ventricle) | right ventricle |
| P5572 | expressed in | ... | Q3064113 (superior frontal gyrus) | superior frontal gyrus |
| P5572 | expressed in | ... | Q223172 (Achilles tendon) | Achilles tendon |
| P5572 | expressed in | ... | Q4973067 (Brodmann area 23) | Brodmann area 23 |
| P5572 | expressed in | ... | Q5407200 (middle temporal gyrus) | middle temporal gyrus |
| P5572 | expressed in | ... | Q11394395 (endothelial cell) | endothelial cell |
| P703 | found in taxon | ... | Q15978631 (Homo sapiens) | Homo sapiens |
| P692 | Gene Atlas image | CommonsMedia | http://commons.wikimedia.org/wiki/Special:FilePath/PBB%20GE%20OPA1%20212213%20x%20at%20fs.png | ??? |
| P692 | Gene Atlas image | CommonsMedia | http://commons.wikimedia.org/wiki/Special:FilePath/PBB%20GE%20OPA1%20212214%20at%20fs.png | ??? |
| P692 | Gene Atlas image | CommonsMedia | http://commons.wikimedia.org/wiki/Special:FilePath/PBB%20GE%20OPA1%20214306%20at%20fs.png | ??? |
| P2293 | genetic association | ... | Q55785034 (mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type); MTDPS14) | mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type); MTDPS14 |
| P2293 | genetic association | ... | Q814547 (Behr syndrome) | Behr syndrome |
| P2293 | genetic association | ... | Q2869820 (Kjer's optic neuropathy) | Kjer's optic neuropathy |
| P2293 | genetic association | ... | Q3629049 (optic atrophy) | optic atrophy |
| P645 | genomic end | String | 193697811 | ??? |
| P645 | genomic end | String | 193415612 | ??? |
| P644 | genomic start | String | 193310933 | ??? |
| P644 | genomic start | String | 193593144 | ??? |
| P593 | HomoloGene ID | String | 14618 | ??? |
| P31 | instance of | ... | Q7187 (gene) | gene |
| P684 | ortholog | ... | Q29767925 (opa1) | opa1 |
| P684 | ortholog | ... | Q18266525 (Opa1) | Opa1 |
| P684 | ortholog | ... | Q24406235 (Opa1) | Opa1 |
| P684 | ortholog | ... | Q29706095 (eat-3) | eat-3 |
| P684 | ortholog | ... | Q29715684 (Opa1) | Opa1 |
| P684 | ortholog | ... | Q29762424 (LOC100307079) | LOC100307079 |
| P2548 | strand orientation | ... | Q22809680 (forward strand) | forward strand |
| P279 | subclass of | ... | Q20747295 (protein-coding gene) | protein-coding gene |
| P594 | Ensembl gene ID | ENSG00000198836 |
| P704 | Ensembl transcript ID | ENST00000361150 |
| P704 | Ensembl transcript ID | ENST00000361510 |
| P704 | Ensembl transcript ID | ENST00000361715 |
| P704 | Ensembl transcript ID | ENST00000361828 |
| P704 | Ensembl transcript ID | ENST00000361908 |
| P704 | Ensembl transcript ID | ENST00000392436 |
| P704 | Ensembl transcript ID | ENST00000392437 |
| P704 | Ensembl transcript ID | ENST00000419435 |
| P704 | Ensembl transcript ID | ENST00000429164 |
| P704 | Ensembl transcript ID | ENST00000434811 |
| P704 | Ensembl transcript ID | ENST00000445863 |
| P704 | Ensembl transcript ID | ENST00000475899 |
| P704 | Ensembl transcript ID | ENST00000482865 |
| P704 | Ensembl transcript ID | ENST00000483516 |
| P704 | Ensembl transcript ID | ENST00000495261 |
| P704 | Ensembl transcript ID | ENST00000495476 |
| P704 | Ensembl transcript ID | ENST00000497189 |
| P704 | Ensembl transcript ID | ENST00000642289 |
| P704 | Ensembl transcript ID | ENST00000642445 |
| P704 | Ensembl transcript ID | ENST00000642593 |
| P704 | Ensembl transcript ID | ENST00000643329 |
| P704 | Ensembl transcript ID | ENST00000643737 |
| P704 | Ensembl transcript ID | ENST00000644595 |
| P704 | Ensembl transcript ID | ENST00000644629 |
| P704 | Ensembl transcript ID | ENST00000644841 |
| P704 | Ensembl transcript ID | ENST00000644959 |
| P704 | Ensembl transcript ID | ENST00000645553 |
| P704 | Ensembl transcript ID | ENST00000646085 |
| P704 | Ensembl transcript ID | ENST00000646277 |
| P704 | Ensembl transcript ID | ENST00000646544 |
| P704 | Ensembl transcript ID | ENST00000646699 |
| P704 | Ensembl transcript ID | ENST00000646793 |
| P351 | Entrez Gene ID | 4976 |
| P4317 | GARD rare disease ID | 9890 |
| P353 | HGNC gene symbol | OPA1 |
| P354 | HGNC ID | 8140 |
| P492 | OMIM ID | 605290 |
| P492 | OMIM ID | 605290 |
| P639 | RefSeq RNA ID | NM_001354663 |
| P639 | RefSeq RNA ID | NM_001354664 |
| P639 | RefSeq RNA ID | NM_015560 |
| P639 | RefSeq RNA ID | NM_130831 |
| P639 | RefSeq RNA ID | NM_130832 |
| P639 | RefSeq RNA ID | NM_130833 |
| P639 | RefSeq RNA ID | NM_130834 |
| P639 | RefSeq RNA ID | NM_130835 |
| P639 | RefSeq RNA ID | NM_130836 |
| P639 | RefSeq RNA ID | NM_130837 |
| P639 | RefSeq RNA ID | XR_001740158 |
| P639 | RefSeq RNA ID | XR_001740159 |
| P2892 | UMLS CUI | C1417953 |
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log id: 4458564