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MIRAGE
hereditary spastic paraplegia 62

Summary
Synonym
  • SPG62
  • autosomal recessive spastic paraplegia 62
  • autosomal recessive spastic paraplegia type 62
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN1 gene on chromosome 10q24.
Super Class
autosomal recessive disease hereditary spastic paraplegia
Disease Ontology
DOID:0110813
Mondo Disease Ontology
ORDO
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
10613 ERLIN1 ER lipid raft associated 1
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
O75477 Erlin-1
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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