melena Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description The passage of blackish, tarry feces associated with gastrointestinal hemorrhage. Melena occurs if the blood remains in the colon long enough for it to be broken down by colonic bacteria. One degradation product, hematin, imbues the stool with a blackish color. Thus, melena generally occurs with bleeding from the upper gastrointestinal tract (e.g., sotmach ulcers or duodenal ulcers), since the blood usually remains in the gut for a longer period of time than with lower gastrointestinal bleeding. (Human Phenotype Ontology, HP_0002249)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003292
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Genes

4 gene mutations causing the melena phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APC adenomatous polyposis coli
FOXP3 forkhead box P3
MUC2 mucin 2, oligomeric mucus/gel-forming
VWF von Willebrand factor