Difference between revisions of "Hemochromatosis 2011"
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| + | == Summary == |
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| + | '''''The example disease causes the example syndrome.''''' |
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| + | |||
Hemochromatosis is a hereditary autosomal recessiv genetic disorder caused by a mutation of the HFE-Gen. It was first describted by [http://en.wikipedia.org/wiki/Armand_Trousseau Armand Trousseau] in 1865 in a report about [http://en.wikipedia.org/wiki/Diabetes_mellitus diabetes]. |
Hemochromatosis is a hereditary autosomal recessiv genetic disorder caused by a mutation of the HFE-Gen. It was first describted by [http://en.wikipedia.org/wiki/Armand_Trousseau Armand Trousseau] in 1865 in a report about [http://en.wikipedia.org/wiki/Diabetes_mellitus diabetes]. |
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Hemochromatosis causes different symptoms like skin discoloration and [http://en.wikipedia.org/wiki/Liver_cirrhosis liver cirrhosis]. |
Hemochromatosis causes different symptoms like skin discoloration and [http://en.wikipedia.org/wiki/Liver_cirrhosis liver cirrhosis]. |
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| − | == |
+ | === Cross-references === |
| + | '''''See also description of this disease in |
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| + | * specific link to Wikipedia |
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| + | * specific link to HGMD |
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| + | * specific link to OMIM |
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| + | ... (see [[Resource data|databases in "resources"]])''''' |
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| + | |||
| + | == Biochemical disease mechanism == |
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| + | '''''The example protein is involved in the example pathway...''''' |
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| + | ''''Ideally, include a graphical pathway representation like this one:'''' |
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| + | |||
| + | ''''(see above: own words, no plagiarism)'''' |
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| + | === Cross-references === |
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| + | '''''* link to KEGG |
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| + | * link to MetaCyc |
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| + | ... see [[Resource data|databases in "resources"]]''''' |
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| + | |||
| + | == HEF-Gene == |
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[[Image:Protein_HFE_PDB_1a6z.png|thumb|Source: http://www.pdb.org/pdb/explore/explore.do?structureId=1A6Z]] |
[[Image:Protein_HFE_PDB_1a6z.png|thumb|Source: http://www.pdb.org/pdb/explore/explore.do?structureId=1A6Z]] |
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The HFE-Gen alleviate the binding of [http://en.wikipedia.org/wiki/Transferrin transferrin] which is the carrier protein for iron in the blood cyclus. |
The HFE-Gen alleviate the binding of [http://en.wikipedia.org/wiki/Transferrin transferrin] which is the carrier protein for iron in the blood cyclus. |
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With a mutated HFE-Gen, the intestines interpret a strong transferrin signal as an deficient in iron. Therefore the cells start to import iron, which leads to an iron |
With a mutated HFE-Gen, the intestines interpret a strong transferrin signal as an deficient in iron. Therefore the cells start to import iron, which leads to an iron |
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overload. |
overload. |
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| − | === Mutation === |
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| − | ==== assigned Sequence 1 ==== |
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| − | under construction 'till sequences are assingned |
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| + | == Mutations == |
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| − | ==== assigned Sequence 2 ==== |
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| + | 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. |
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| − | under construction 'till sequences are assingned |
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| + | |||
| + | === Reference sequence === |
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| + | |||
| + | Which sequence does not cause the disease and is most often found in the population. |
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| + | * [[example_sequence|Create a page for the reference sequence.]] |
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| + | |||
| + | === Neutral mutations === |
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| + | * [[example_sequence|Create one page per mutated sequence]]. |
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| + | |||
| + | === Disease causing mutations === |
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| + | * [[example_sequence|Create one page per mutated sequence]]. |
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Revision as of 18:28, 15 May 2011
Contents
Summary
The example disease causes the example syndrome.
Hemochromatosis is a hereditary autosomal recessiv genetic disorder caused by a mutation of the HFE-Gen. It was first describted by Armand Trousseau in 1865 in a report about diabetes.
Phenotype
Hemochromatosis causes different symptoms like skin discoloration and liver cirrhosis.
Cross-references
See also description of this disease in
- specific link to Wikipedia
- specific link to HGMD
- specific link to OMIM
... (see databases in "resources")
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"
HEF-Gene
The HFE-Gen alleviate the binding of transferrin which is the carrier protein for iron in the blood cyclus. With a mutated HFE-Gen, the intestines interpret a strong transferrin signal as an deficient in iron. Therefore the cells start to import iron, which leads to an iron overload.
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.
Reference sequence
Which sequence does not cause the disease and is most often found in the population.
