Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
congenital disorder of glycosylation Ik
Summary
- Synonym
-
- congenital disorder of glycosylation 1k
- Definition
- A congenital disorder of glycosylation I that is characterized by severe developmental and psychomotor delay, muscular hypotonia, intractable early-onset seizures, and microcephaly and has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding beta-1,4-mannosyltransferase on chromosome 16p13.
- Super Class
- autosomal recessive disease congenital disorder of glycosylation type I
External Links
- Disease Ontology
- DOID:0080563
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
Related Genes
| Gene ID | Gene Symbol | Description | Source | Organism |
|---|---|---|---|---|
| 594994 | alg1 | ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase | Xenopus tropicalis (tropical clawed frog) | |
| 100037043 | alg1.L | ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase L homeolog | Xenopus laevis (African clawed frog) |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9BT22 | Chitobiosyldiphosphodolichol beta-mannosyltransferase |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002721 | Immunodeficiency |
| HP:0001250 | Seizure |
| HP:0011024 | Abnormality of the gastrointestinal tract |
| HP:0001272 | Cerebellar atrophy |
| HP:0000486 | Strabismus |
| HP:0002059 | Cerebral atrophy |
| HP:0000077 | Abnormality of the kidney |
| HP:0001627 | Abnormal heart morphology |
| HP:0002719 | Recurrent infections |
| HP:0001249 | Intellectual disability |
