8csw: Difference between revisions

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== Disease ==
== Disease ==
[[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN]] Hereditary spherocytosis. The disease is caused by variants affecting the gene represented in this entry.  
[[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN]] Hereditary spherocytosis. The disease is caused by variants affecting the gene represented in this entry.
== Function ==
== Function ==
[[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN]] Probably plays an important role in the regulation of erythrocyte shape and mechanical properties.  
[[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN]] Probably plays an important role in the regulation of erythrocyte shape and mechanical properties.
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== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Large Structures]]
[[Category: Cali, T]]
[[Category: Cali T]]
[[Category: Clarke, O B]]
[[Category: Clarke OB]]
[[Category: Johnston, J D]]
[[Category: Johnston JD]]
[[Category: Kim, K]]
[[Category: Kim K]]
[[Category: Noble, A J]]
[[Category: Noble AJ]]
[[Category: Vallese, F]]
[[Category: Vallese F]]
[[Category: Yen, L Y]]
[[Category: Yen LY]]
[[Category: Anion exchange]]
[[Category: Erythrocyte]]
[[Category: Glycoprotein]]
[[Category: Membrane protein]]
[[Category: Transport protein-structural protein complex]]