Division of Molecular and Cellular Biology (NHO Tokyo Medical Center)
General information
Division of Molecular and Cellular Biology
NHO Tokyo Medical Center
2-5-1 Higashigaoka, Meguro-ku
Tokyo
Japan - 152-8902
https://iwatalab.org/index.html
Organization ID: 508765
NHO Tokyo Medical Center
2-5-1 Higashigaoka, Meguro-ku
Tokyo
Japan - 152-8902
https://iwatalab.org/index.html
Organization ID: 508765
Assertion criteria
Level: Assertion criteria not provided
Summary of submissions to ClinVar
Total submissions: 20
Gene
| Gene | Submissions | Last Updated |
|---|---|---|
| ABCA4 | 2 | Oct 10, 2022 |
| ABHD12 | 1 | Oct 10, 2022 |
| AGBL5 | 1 | Oct 10, 2022 |
| CACNA1F | 5 | Oct 10, 2022 |
| GPHN | 1 | Oct 10, 2022 |
| GRK1 | 1 | Oct 10, 2022 |
| LOC126863257 | 1 | Oct 10, 2022 |
| NYX | 2 | Oct 10, 2022 |
| OPA1 | 1 | Oct 10, 2022 |
| PDE6C | 1 | Oct 10, 2022 |
| RDH12 | 1 | Oct 10, 2022 |
| RLBP1 | 1 | Oct 10, 2022 |
| RPGR | 2 | Oct 10, 2022 |
| TOPORS | 1 | Oct 10, 2022 |
| USH2A | 1 | Oct 10, 2022 |
| USH2A-AS1 | 1 | Oct 10, 2022 |
Condition
| Name | Submissions | Last Updated |
|---|---|---|
| Autosomal dominant optic atrophy classic form | 1 | Oct 10, 2022 |
| Cone dystrophy 4 | 1 | Oct 10, 2022 |
| Congenital stationary night blindness 1A | 2 | Oct 10, 2022 |
| Congenital stationary night blindness 2A | 5 | Oct 10, 2022 |
| Leber congenital amaurosis 13 | 1 | Oct 10, 2022 |
| Oguchi disease-2 | 1 | Oct 10, 2022 |
| PHARC syndrome | 1 | Oct 10, 2022 |
| Pigmentary retinal dystrophy | 1 | Oct 10, 2022 |
| Retinitis pigmentosa 3 | 1 | Oct 10, 2022 |
| Retinitis pigmentosa 31 | 1 | Oct 10, 2022 |
| Retinitis pigmentosa 39 | 1 | Oct 10, 2022 |
| Retinitis pigmentosa 75 | 1 | Oct 10, 2022 |
| Severe early-childhood-onset retinal dystrophy | 2 | Oct 10, 2022 |
| X-linked cone-rod dystrophy 1 | 1 | Oct 10, 2022 |