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MIRAGE
primary localized cutaneous amyloidosis 1

Summary
Synonym
  • familial primary localized cutaneous amyloidosis-1
Definition
A primary cutaneous amyloidosis that has_material_basis_in heterozygous mutation in the gene encoding oncostatin M receptor-beta (OSMR) on chromosome 5p13.
Super Class
primary cutaneous amyloidosis
Disease Ontology
DOID:0080930
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9180 OSMR oncostatin M receptor
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q99650 Oncostatin-M-specific receptor subunit beta
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 8, 2025