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BRIDGE_SPEED_NEURO_v2.0_20160416

Gene: GNAL

Red List (low evidence)

GNAL (G protein subunit alpha L)
EnsemblGeneIds (GRCh38): ENSG00000141404
EnsemblGeneIds (GRCh37): ENSG00000141404
OMIM: 139312, Gene2Phenotype
GNAL is in 6 panels

1 review

BRIDGE consortium (NIHRBR-RD)

Green List (high evidence)

manju_list; neuro_20160418_strict; NA
Created: 7 Feb 2017, 4:28 p.m.

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Phenotypes
Dystonia 25, 615073

Variants in this GENE are reported as part of current diagnostic practice

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • BRIDGE
Phenotypes
  • Dystonia 25, 615073
OMIM
139312
Clinvar variants
Variants in GNAL
Penetrance
Complete
Panels with this gene

History Filter Activity

7 Feb 2017, Gel status: 0

Created

Ellen McDonagh (Genomics England Curator)

GNAL was created by ellenmcdonagh

7 Feb 2017, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

GNAL was added to BRIDGE_SPEED_NEURO_v2.0_20160416panel. Sources: BRIDGE