hereditary spastic paraplegia 12

Summary
Synonym
  • SPG12
  • autosomal dominant spastic paraplegia 12
  • autosomal dominant spastic paraplegia type 12
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13.
Super Class
autosomal dominant disease hereditary spastic paraplegia
Related Genes
Displaying all 4 entries
Gene ID Gene Symbol Description Source
6252 RTN1 reticulon 1
6253 RTN2 reticulon 2
10313 RTN3 reticulon 3
57142 RTN4 reticulon 4
Displaying all 3 entries
Gene ID Gene Symbol Description Source
20168 Rtn3 reticulon 3
68585 Rtn4 reticulon 4
104001 Rtn1 reticulon 1

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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