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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
fundus albipunctatus
Summary
- Synonym
-
- Pigmentary retinal dystrophy
- retinitis punctata albescens
- Definition
- A fundus dystrophy that is characterized by discrete uniform white dots over the entire fundus with greatest density in the midperiphery and no macular involvement.
- Super Class
- fundus dystrophy
External Links
- Disease Ontology
- DOID:11105
- Mondo Disease Ontology
- MeSH
- UMLS
- OMIM
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 3099 | HK2 | hexokinase 2 | |
| 3418 | IDH2 | isocitrate dehydrogenase (NADP(+)) 2 | |
| 3419 | IDH3A | isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha | |
| 3420 | IDH3B | isocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit beta | |
| 3612 | IMPA1 | inositol monophosphatase 1 | |
| 4190 | MDH1 | malate dehydrogenase 1 | |
| 4669 | NAGLU | N-acetyl-alpha-glucosaminidase | |
| 5160 | PDHA1 | pyruvate dehydrogenase E1 subunit alpha 1 | |
| 5373 | PMM2 | phosphomannomutase 2 | |
| 5621 | PRNP | prion protein (Kanno blood group) |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9UJJ9 | N-acetylglucosamine-1-phosphotransferase subunit gamma | |
| Q9UKY4 | Protein O-mannosyl-transferase 2 | |
| Q9UQE7 | Structural maintenance of chromosomes protein 3 | |
| Q9Y5P6 | Mannose-1-phosphate guanyltransferase beta | |
| Q9Y6A1 | Protein O-mannosyl-transferase 1 |
