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GMS Neurology specialist test group-Movement disorders - childhood onset-LNGLH_v2

Gene: GPAA1

Red List (low evidence)

GPAA1 (glycosylphosphatidylinositol anchor attachment 1)
EnsemblGeneIds (GRCh38): ENSG00000197858
EnsemblGeneIds (GRCh37): ENSG00000197858
OMIM: 603048, Gene2Phenotype
GPAA1 is in 10 panels

1 review

James Polke (Neurogenetics Laboratory, Institute of Neurology, London)

Red List (low evidence)

History Filter Activity

5 Apr 2019, Gel status: 1

Added New Source

Louise Daugherty (Genomics England Curator)

Source Expert Review Red was added to GPAA1.

5 Apr 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance

Louise Daugherty (Genomics England Curator)

gene: GPAA1 was added gene: GPAA1 was added to GMS Neurology specialist test group-Movement disorders - childhood onset-LNGLH_v2. Sources: London North GLH Mode of inheritance for gene: GPAA1 was set to