LARGE xylosyl- and glucuronyltransferase 1

Summary
Gene Symbol
  • LARGE1
Aliases
  • KIAA0609
  • like-acetylglucosaminyltransferase
Organism
Homo sapiens (human)
External Links
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
Reactions
Displaying all 4 entries
Donor Acceptor Product Reference
UDP-Xyl
G42293RF
UDP-GlcA
G16579HJ
UDP-GlcA
G42293RF
UDP-Xyl
G16579HJ
Displaying all 4 entries
Donor Acceptor Product Reference
UDP-Xyl
G16579HJ
UDP-GlcA
G42293RF
UDP-GlcA
G16579HJ
UDP-Xyl
G42293RF
Orthologous Gene
Displaying all 2 entries
Species Protein mRNA
Caenorhabditis elegans NP_509833 NM_077432
Mus musculus NP_034817 NM_010687
KEGG BRITE Database
Orthology
K09668
Name
glycosyltransferase-like protein LARGE [EC:2.4.2.- 2.4.1.-]
References
Disease
Disease Ontology
Displaying entries 1 - 10 of 172 in total
DO ID Disease Name Source
DOID:0050453 lissencephaly
DOID:0050557 congenital muscular dystrophy
DOID:0050559 Fukuyama congenital muscular dystrophy
DOID:0050560 Walker-Warburg syndrome
DOID:0050572 cone-rod dystrophy
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1
DOID:0050777 Joubert syndrome
DOID:0060249 scoliosis
DOID:0060250 idiopathic scoliosis
DOID:0060255 rippling muscle disease 2
The Human Phenotype Ontology
Displaying entries 1 - 10 of 151 in total
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000028 Cryptorchidism
HP:0000050 Hypoplastic male external genitalia
HP:0000054 Micropenis
HP:0000110 Renal dysplasia
HP:0000158 Macroglossia
HP:0000175 Cleft palate
HP:0000176 Submucous cleft hard palate
HP:0000193 Bifid uvula
HP:0000204 Cleft upper lip
Displaying all 6 entries
Disease ID Disease Name
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: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
OMIM:608840
  • muscular dystrophy-dystroglycanopathy type B6
OMIM:236670
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
ORPHA:588
  • muscle-eye-brain disease
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1

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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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