LARGE1 Chromosome 22

LARGE xylosyl- and glucuronyltransferase 1
67 variants 67 Health Risk

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What This Gene Does
This gene encodes a member of the N-acetylglucosaminyltransferase gene family. It encodes a glycosyltransferase which participates in glycosylation of alpha-dystroglycan, and may carry out the synthesis of glycoprotein and glycosphingolipid sugar chains. It may also be involved in the addition of a repeated disaccharide unit. The protein encoded by this gene is the glycotransferase that adds the final xylose and glucuronic acid to alpha-dystroglycan and thereby allows alpha-dystroglycan to bind ligands including laminin 211 and neurexin. Mutations in this gene cause several forms of congenital muscular dystrophy characterized by cognitive disability and abnormal glycosylation of alpha-dystroglycan. Alternative splicing of this gene results in multiple transcript variants that encode the same protein. [provided by RefSeq, May 2018]
Gene Info
Gene Group
"Glycosyltransferase family 8|MicroRNA protein coding host genes"
Locus Type
gene with protein product
Location
22q12.3
Ensembl
ENSG00000133424
Associated Conditions (9)
Muscular dystrophy-dystroglycanopathy type B6
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A6
Muscular dystrophy
type A1
LARGE1-related disorder
Inborn genetic diseases
Retinitis pigmentosa
LARGE1-Related Disorders
Key Variants
RS113253213
Conflicting classifications of pathogenicity
Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
Health Risk
RS115686643
Conflicting classifications of pathogenicity
Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
Health Risk
RS116164106
Conflicting classifications of pathogenicity
Muscular dystrophy, Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
Health Risk
RS1257326994
Conflicting classifications of pathogenicity
Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
Health Risk
RS12627793
Conflicting classifications of pathogenicity
Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
Health Risk
RS141089495
Conflicting classifications of pathogenicity
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6, Muscular dystrophy-dystroglycanopathy type B6
Health Risk
RS1414312676
Conflicting classifications of pathogenicity
Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
Health Risk
RS141818070
Conflicting classifications of pathogenicity
Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
Health Risk
RS144045461
Conflicting classifications of pathogenicity
Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
Health Risk
RS144216539
Conflicting classifications of pathogenicity
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6, Muscular dystrophy-dystroglycanopathy type B6
Health Risk
RS145048151
Conflicting classifications of pathogenicity
Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
Health Risk
RS146552975
Conflicting classifications of pathogenicity
Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
Health Risk
All Variants (67)
RSID Category Clinical Significance Conditions
RS2065252717 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
RS2080768582 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
RS2080771312 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
RS2145893296 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
RS2148785084 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
RS2519156797 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
RS2520889050 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
RS2546646656 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
RS2546646853 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
RS2546647342 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
RS2547094272 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
RS267607209 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6, Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
RS267607210 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6, Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
RS398124181 Health Risk Pathogenic
RS761071115 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6, Muscular dystrophy-dystroglycanopathy type B6
RS772985451 Health Risk Pathogenic Muscular dystrophy-dystroglycanopathy type B6, Muscular dystrophy-dystroglycanopathy type B6
RS121908675 Health Risk Pathogenic/Likely pathogenic Muscular dystrophy-dystroglycanopathy type B6, LARGE1-Related Disorders, Muscular dystrophy-dystroglycanopathy type B6
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