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
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
10613 ERLIN1 ER lipid raft associated 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
226144 Erlin1 ER lipid raft associated 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
541490 erlin1 ER lipid raft associated 1
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
549646 erlin1 ER lipid raft associated 1 Xenopus tropicalis (tropical clawed frog)
Displaying 1 entry
Gene ID Gene Symbol Description Source
178178 erl-1 Erlin

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: December 9, 2024