8csw
From Proteopedia
(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. |
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== 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 | + | [[Category: Cali T]] |
| - | [[Category: Clarke | + | [[Category: Clarke OB]] |
| - | [[Category: Johnston | + | [[Category: Johnston JD]] |
| - | [[Category: Kim | + | [[Category: Kim K]] |
| - | [[Category: Noble | + | [[Category: Noble AJ]] |
| - | [[Category: Vallese | + | [[Category: Vallese F]] |
| - | [[Category: Yen | + | [[Category: Yen LY]] |
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Revision as of 04:50, 8 September 2022
Local refinement of protein 4.2 in Class 2 of erythrocyte ankyrin-1 complex
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Categories: Homo sapiens | Large Structures | Cali T | Clarke OB | Johnston JD | Kim K | Noble AJ | Vallese F | Yen LY
