Difference between revisions of "Example/Template"
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(Describe this in your own words, avoid plagiarism. Summarise the information from different sources.) |
(Describe this in your own words, avoid plagiarism. Summarise the information from different sources.) |
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+ | The disesase is also described in detail at |
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− | === Cross-references === |
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+ | * [http://en.wikipedia.org/wiki/Iron_overload] |
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− | See also description of this disease in |
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+ | * [http://www.hgmd.cf.ac.uk/ac/gene.php?gene=HFE] |
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− | * specific link to Wikipedia |
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+ | * [http://www.ncbi.nlm.nih.gov/omim/235200] |
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− | * specific link to HGMD |
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+ | * [http://www.ncbi.nlm.nih.gov/pubmed/21510925] |
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− | * specific link to OMIM |
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+ | * [http://www.nlm.nih.gov/medlineplus/hemochromatosis.html] |
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− | ... (see [[Resource data|databases in "resources"]]) |
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+ | * [http://digestive.niddk.nih.gov/ddiseases/pubs/hemochromatosis] |
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+ | * [http://www.hemochromatosis.org] |
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== Biochemical disease mechanism == |
== Biochemical disease mechanism == |
Revision as of 18:47, 15 May 2011
Contents
Summary
The example disease causes the example syndrome.
Phenotype
Phenotypic description of the disease.
(Describe this in your own words, avoid plagiarism. Summarise the information from different sources.)
The disesase is also described in detail at
Biochemical disease mechanism
The example protein is involved in the example pathway...
Ideally, include a graphical pathway representation like this one:
(see above: own words, no plagiarism)
Cross-references
- link to KEGG
- link to MetaCyc
... see databases in "resources"
Mutations
Current knowledge about mutations associated with the disease. - Separate into disease causing and neutral mutations. -- These sequence pages will be the starting point for collecting prediction results and result discussions.
Note: Currently (13.5.) you only need to care about the reference sequence pages. -- At a later stage we will assign mutations we expect you to work on. Then, it will make sense to create on page per mutation that is assigned to you.
Reference sequence
Which sequence does not cause the disease and is most often found in the population.