Hereditary spastic paraplegia - adult onset
Gene: AP4M1
Appears to be childhood onset only. Few patients reported but sufficient to show association.Created: 3 May 2019, 4:13 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Publications
Variants in this GENE are reported as part of current diagnostic practice
Green gene with Amber GLH rating, Gene discussed in view of discrepant rating(s) from GLH(s). Green rating agreed at the GMS Neurology Specialist Test Group Webex on 17th May 2019.Created: 21 May 2019, 4:14 p.m.
Review and rating submitted byJames Polke (Neurogenetics Laboratory,Institute of Neurology, London), unless specified in the review comment, on behalf of London North GLH for GMS Neurology specialist test group.Created: 9 May 2019, 4:50 p.m.
Victoria-childhood onset. In Sheffields HSP panelCreated: 25 Apr 2019, 1:22 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spastic paraplegia 50, autosomal recessive, 612936
Publications for gene: AP4M1 were set to
Source Yorkshire and North East GLH was added to AP4M1.
Source Expert Review Green was added to AP4M1. Mode of inheritance for gene AP4M1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Spastic paraplegia 50, autosomal recessive, 612936 for gene: AP4M1 Rating Changed from Red List (low evidence) to Green List (high evidence)
Source NHS GMS was added to AP4M1.
gene: AP4M1 was added gene: AP4M1 was added to Hereditary spastic paraplegia - adult onset. Sources: London North GLH Mode of inheritance for gene: AP4M1 was set to