Difference between revisions of "Template:Disorders of translation and posttranslational modification"
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imported>Arcadian (3-Methylglutaconic aciduria) |
imported>Frietjes m (copyedit) |
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{{Navbox | {{Navbox | ||
| − | |name | + | | name = Disorders of translation and posttranslational modification |
| − | |title | + | | title = Disorders of [[Eukaryotic translation|translation]] and [[posttranslational modification]] |
| + | | bodyclass = hlist | ||
| titlestyle = background:Silver | | titlestyle = background:Silver | ||
| − | |group1 | + | | group1 = Translation |
| − | |list1 | + | | list1 = |
| + | * [[Ribosome]]: [[Diamond–Blackfan anemia]] | ||
| + | * ''[[FMR1]]'' | ||
| + | ** [[Fragile X syndrome]] | ||
| + | ** [[Fragile X-associated tremor/ataxia syndrome]] | ||
| + | ** [[Premature ovarian failure|Premature ovarian failure 1]] | ||
| − | [[Initiation factor]]: [[Leukoencephalopathy with vanishing white matter]] | + | * [[Initiation factor]]: [[Leukoencephalopathy with vanishing white matter]] |
| − | [[snRNP]]: [[Retinitis pigmentosa|Retinitis pigmentosa 33]] | + | * [[snRNP]]: [[Retinitis pigmentosa|Retinitis pigmentosa 33]] |
| − | |group2 | + | | group2 = Posttranslational modification |
| − | |list2 | + | | list2 = |
| − | | | + | {{Navbox|subgroup |
| − | | | + | | group1 = [[Protein folding]] |
| + | | list1 = | ||
| + | * [[Alzheimer's disease]] | ||
| + | * [[Huntington's disease]] | ||
| + | * [[Creutzfeldt–Jakob disease]] | ||
| + | * chaperonins: [[3-Methylglutaconic aciduria|3-Methylglutaconic aciduria 5]] | ||
| − | | | + | | group2 = [[Protein targeting]] |
| − | | | + | | list2 = |
| + | * [[I-cell disease]] | ||
| − | + | | group3 = [[Ubiquitin]] | |
| + | | list3 = | ||
| + | * [[Ubiquitin-activating enzyme|E1]]: [[X-linked spinal muscular atrophy 2]] | ||
| − | | | + | * [[Ubiquitin ligase|E3]]: [[Johanson–Blizzard syndrome]] |
| − | + | * [[Von Hippel–Lindau disease]] | |
| + | * [[3-M syndrome]] | ||
| + | * [[Angelman syndrome]] | ||
| − | + | * [[Deubiquitinating enzyme]]: [[Machado–Joseph disease]] | |
| − | + | * [[Aneurysmal bone cyst]] | |
| + | * [[Multiple familial trichoepithelioma|Multiple familial trichoepithelioma 1]] | ||
| − | + | | group4 = [[Small ubiquitin-related modifier 1|SUMO]] | |
| + | | list4 = | ||
| + | * [[Cleft lip and palate|OFC10]] | ||
| − | [[ | + | | group5 = Other |
| + | | list5 = | ||
| + | * [[Multiple sulfatase deficiency]] | ||
| + | * [[Hyperproinsulinemia]] | ||
| + | * [[Ehlers–Danlos syndrome|Ehlers–Danlos syndrome 6]] | ||
| + | }} | ||
| − | | | + | | below = |
| − | + | ;See also | |
| − | + | : [[Template:Genetic translation|genetic translation]] | |
| − | + | : [[Template:Posttranslational modification|posttranslational modification]] | |
| − | + | {{Protein defects by function navs}} | |
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}}<noinclude> | }}<noinclude> | ||
[[Category:Disorders of synthesis of DNA, RNA, and proteins]] | [[Category:Disorders of synthesis of DNA, RNA, and proteins]] | ||
[[Category:Genetic disease and disorder templates by mechanism]] | [[Category:Genetic disease and disorder templates by mechanism]] | ||
</noinclude> | </noinclude> | ||