Genes in panel
STRs in panel
Prev Next
Regions in panel
Prev Next

BRIDGE_SPEED_NEURO_v2.0_20160416

Gene: AGL

Red List (low evidence)

AGL (amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase)
EnsemblGeneIds (GRCh38): ENSG00000162688
EnsemblGeneIds (GRCh37): ENSG00000162688
OMIM: 610860, Gene2Phenotype
AGL is in 16 panels

1 review

BRIDGE consortium (NIHRBR-RD)

Green List (high evidence)

ddg2p_20141118; ddg2p_20141118_conf; ddg2p_201507; ddg2p_201507_conf; neuro_20160418_strict; Loss of function
Created: 7 Feb 2017, 4:09 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Glycogen storage disease IIIa, 232400; Glycogen storage disease; IIIb, 232400;

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

History Filter Activity

7 Feb 2017, Gel status: 0

Created

Ellen McDonagh (Genomics England Curator)

AGL was created by ellenmcdonagh

7 Feb 2017, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

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