congenital muscular dystrophy-dystroglycanopathy type A3

Summary
Synonym
  • MDDGA3
  • Walker-Warburg syndrome or muscle-eye-brain disease, POMGNT1-related
  • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A3
Definition
A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in POMGNT1 on 1p34.1.
Super Class
congenital muscular dystrophy-dystroglycanopathy type A
Disease Ontology
DOID:0111236
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
55624 POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
Displaying 1 entry
Gene ID Gene Symbol Description Source
68273 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source
362567 Pomgnt1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
Displaying 1 entry
Gene ID Gene Symbol Description Source
571876 pomgnt1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
Displaying all 3 entries
Gene ID Gene Symbol Description Source Organism
414570 pomgnt1.L protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) L homeolog Xenopus laevis (African clawed frog)
495292 pomgnt1.S protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) S homeolog Xenopus laevis (African clawed frog)
100158594 pomgnt1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) Xenopus tropicalis (tropical clawed frog)
The Human Phenotype Ontology
Displaying entries 61 - 70 of 98 in total
HPO ID HPO Term
HP:0003457 EMG abnormality
HP:0004374 Hemiplegia/hemiparesis
HP:0007360 Aplasia/Hypoplasia of the cerebellum
HP:0100022 Abnormality of movement
HP:0100543 Cognitive impairment
HP:0000007 Autosomal recessive inheritance
HP:0000232 Everted lower lip vermilion
HP:0000272 Malar flattening
HP:0000347 Micrognathia
HP:0000485 Megalocornea
Displaying entries 1 - 10 of 14 in total
Gene ID Gene Symbol Description
10329 RXYLT1 ribitol xylosyltransferase 1
10585 POMT1 protein O-mannosyltransferase 1
11041 B4GAT1 beta-1,4-glucuronyltransferase 1
148789 B3GALNT2 beta-1,3-N-acetylgalactosaminyltransferase 2
1605 DAG1 dystroglycan 1
2218 FKTN fukutin
29925 GMPPB GDP-mannose pyrophosphorylase B
29954 POMT2 protein O-mannosyltransferase 2
55624 POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
729920 CRPPA CDP-L-ribitol pyrophosphorylase A

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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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Last updated: December 9, 2024