Hereditary spastic paraplegia

Gene: SPG27

No list

SPG27 (spastic paraplegia 27 (autosomal recessive))
OMIM: 609041, Gene2Phenotype
SPG27 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, 2:26 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, 4:29 p.m.

emma baple (Genomics England Curator)

Red List (low evidence)

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Removed
  • Expert list
Tags
locus-type-phenotype-only
OMIM
609041
Clinvar variants
Variants in SPG27
Penetrance
Complete
Publications
  • Meijer IA et al. (2004)
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.

9 Mar 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

Added New Source

Ellen McDonagh (Genomics England Curator)

SPG27 was added to Hereditary spastic paraplegiapanel. Sources: Expert list