EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   3.1.1.64 | Acne Vulgaris |
15218101 |
The specific binding of retinoic acid to RPE65 and approaches to the treatment of macular degeneration. |
diagnostic usage
therapeutic application
unassigned |
3
4
0 |
| 3.1.1.64 | Adenocarcinoma |
31516576 |
Bioinformatics and functional analyses of key genes in smoking-associated lung adenocarcinoma. |
diagnostic usage
ongoing research
therapeutic application
unassigned |
3
3
1
0 |
| 3.1.1.64 | Blindness |
9326927 |
Mutations in RPE65 cause Leber's congenital amaurosis. |
causal interaction
unassigned |
3
0 |
| 3.1.1.64 | Blindness |
9501220 |
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. |
causal interaction
unassigned |
3
0 |
| 3.1.1.64 | Blindness |
9843205 |
Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle. |
causal interaction
unassigned |
4
0 |
| 3.1.1.64 | Blindness |
10090910 |
Different functional outcome of RetGC1 and RPE65 gene mutations in Leber congenital amaurosis. |
ongoing research
unassigned |
1
0 |
| 3.1.1.64 | Blindness |
10766140 |
Mutation analysis of 3 genes in patients with Leber congenital amaurosis. |
diagnostic usage
unassigned |
3
0 |
| 3.1.1.64 | Blindness |
10869443 |
Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindness. |
unassigned |
0 |
| 3.1.1.64 | Blindness |
11062306 |
A homozygous deletion in RPE65 in a small Sardinian family with autosomal recessive retinal dystrophy. |
causal interaction
diagnostic usage
unassigned |
1
3
0 |
| 3.1.1.64 | Blindness |
11139690 |
[Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes] |
causal interaction
unassigned |
3
0 |
