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 |