muscular dystrophy-dystroglycanopathy type B1

Summary
Synonym
  • CMD due to dystroglycanopathy
  • Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1
Definition
A congenital muscular dystrophy characterized by muscle weakness, cognitive impairment and brain abnormalities and has_material_basis_in mutation to the POMT1 gene that encodes O-mannosyltransferase.
Super Class
autosomal recessive disease muscular dystrophy-dystroglycanopathy type B
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
10585 POMT1 protein O-mannosyltransferase 1
Displaying all 6 entries
Gene ID Gene Symbol Description Source
16795 Large1 LARGE xylosyl- and glucuronyltransferase 1
68273 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase
99011 Pomt1 protein-O-mannosyltransferase 1
108902 B4gat1 beta-1,4-glucuronyltransferase 1
243853 Fkrp fukutin related protein
246179 Fktn fukutin
Displaying 1 entry
Gene ID Gene Symbol Description Source
571426 fkrp fukutin related protein
The Human Phenotype Ontology
Displaying entries 1 - 10 of 86 in total
HPO ID HPO Term
HP:0000158 Macroglossia
HP:0000238 Hydrocephalus
HP:0000252 Microcephaly
HP:0000485 Megalocornea
HP:0000486 Strabismus
HP:0000518 Cataract
HP:0000525 Abnormality iris morphology
HP:0000541 Retinal detachment
HP:0000545 Myopia
HP:0000568 Microphthalmia
Displaying all 7 entries
Gene ID Gene Symbol Description
29954 POMT2 protein O-mannosyltransferase 2
10585 POMT1 protein O-mannosyltransferase 1
29925 GMPPB GDP-mannose pyrophosphorylase B
79147 FKRP fukutin related protein
9215 LARGE1 LARGE xylosyl- and glucuronyltransferase 1
55624 POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
84197 POMK protein O-mannose kinase

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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: April 7, 2025