Hereditary spastic paraplegia

Gene: SPG32

No list

SPG32 (spastic paraplegia 32 (autosomal recessive))
OMIM: 611252, Gene2Phenotype
SPG32 is in 1 panel

3 reviews

Louise Daugherty (Genomics England Curator)

Comment on list classification: demoted to Grey, this is a phenotype locus type symbol
Created: 15 Aug 2017, 2:24 p.m.

Ellen McDonagh (Genomics England Curator)

Added tag to explain why there is no Ensembl gene ID for this entity.
Created: 9 Jan 2017, 4:31 p.m.

emma baple (Genomics England Curator)

Comment when marking as ready: limited evidence
Created: 10 May 2016, 2:01 p.m.

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Removed
  • Expert list
Tags
locus-type-phenotype-only
OMIM
611252
Clinvar variants
Variants in SPG32
Penetrance
Complete
Publications
  • Stevanin G
Panels with this gene

History Filter Activity

15 Aug 2017, Gel status: 0

Gene classified by Genomics England curator

Louise Daugherty (Genomics England Curator)

This gene has been removed from the panel.

10 May 2016, Gel status: 1

Gene classified by Genomics England curator

emma baple (Genomics England Curator)

This gene has been classified as Red List (Low Evidence).

20 Jul 2015, Gel status: 0

Set Mode of Inheritance

Ellen McDonagh (Genomics England Curator)

Model of inheritance for gene SPG32 was changed to BIALLELIC, autosomal or pseudoautosomal

20 Jul 2015, Gel status: 0

Set Mode of Inheritance

Ellen McDonagh (Genomics England Curator)

Model of inheritance for gene SPG32 was changed to BIALLELIC, autosomal or pseudoautosomal

20 Jul 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

SPG32 was added to Hereditary spastic paraplegiapanel. Sources: Expert list