LARGE xylosyl- and glucuronyltransferase 1

Summary
Gene Symbol
  • LARGE1
Aliases
  • KIAA0609
  • like-acetylglucosaminyltransferase
Organism
Homo sapiens (human)
NCBI Gene
9215
GGDB ID
HGNC
6511
mRNA
map
  • 22q12.3
Protein
OMIM
KEGG Gene ID
hsa:9215
PubChem
9215
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Coiled coil
  • Congenital muscular dystrophy
  • Disease variant
  • Dystroglycanopathy
  • Glycoprotein
  • Glycosyltransferase
  • Golgi apparatus
  • Lissencephaly
  • Manganese
  • Metal-binding
  • Multifunctional enzyme
  • Reference proteome
  • Signal-anchor
  • Transferase
  • Transmembrane helix
Proteins
Displaying all 2 entries
UniProt Protein Name
X5DR28
O95461
  • Acetylglucosaminyltransferase-like 1A
  • Glycosyltransferase-like protein
  • LARGE xylosyl- and glucuronyltransferase 1
Gene Ontology (GO)
GO Hierarchy
GlycoGene Database (GGDB)
GGDB ID
gg171
Gene Symbol
  • LARGE1
Orthologous Gene
Displaying all 2 entries
Species Protein mRNA
Mus musculus NP_034817 NM_010687
Caenorhabditis elegans NP_509833 NM_077432
KEGG BRITE Database
Orthology
K09668
Name
glycosyltransferase-like protein LARGE [EC:2.4.2.- 2.4.1.-]
References
Disease
Disease Ontology
Displaying all 4 entries
DO ID Disease Name Source
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1
DOID:0110637 muscular dystrophy-dystroglycanopathy type B6
DOID:0111242 congenital muscular dystrophy-dystroglycanopathy type A6
DOID:11727 facioscapulohumeral muscular dystrophy
The Human Phenotype Ontology
Displaying entries 21 - 30 of 151 in total
HPO ID HPO Term
HP:0000478 Abnormality of the eye
HP:0000482 Microcornea
HP:0000485 Megalocornea
HP:0000486 Strabismus
HP:0000501 Glaucoma
HP:0000505 Visual impairment
HP:0000518 Cataract
HP:0000519 Developmental cataract
HP:0000528 Anophthalmia
HP:0000541 Retinal detachment
Displaying all 6 entries
Disease ID Disease Name
OMIM:236670
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
OMIM:608840
  • muscular dystrophy-dystroglycanopathy type B6
OMIM:613154
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
ORPHA:899
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
  • muscular dystrophy-dystroglycanopathy, type A
ORPHA:588
  • muscle-eye-brain disease
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
ORPHA:370968
  • congenital muscular dystrophy with intellectual disability
  • muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1
  • muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14
  • muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2
  • muscular dystrophy-dystroglycanopathy type B5
  • muscular dystrophy-dystroglycanopathy type B6

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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