01
Congenital Disorder of Glycosylation, Type In
congenital disorder of glycosylation, type in
congenital disorder of glycosylation, type in
- Entity Type
- Targets
- Relation Groups
- 5
- Relation Preview
- 25
Basic Information
Grouped by core information, identifiers, and descriptions.
Core Information
- Gene Symbol
- ALG5
- Protein Name
- ALG5 dolichyl-phosphate beta-glucosyltransferase
- Gene Type
- protein-coding
- Chromosome
- 13
- Map Location
- 13q13.3
Identifiers
- Entrez ID
- 29880
- Ensembl ID
- ENSG00000120697
- UniProt ID
- No data
- HGNC ID
- No data
- PDB ID
- No data
Description and Extensions
- Description
- No data
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Diseases
target disease4 Diseases
02
Congenital Disorders of Glycosylation
congenital disorders of glycosylation
congenital disorders of glycosylation
03
04
Pontocerebellar Hypoplasia, Type 1C
pontocerebellar hypoplasia, type 1c
pontocerebellar hypoplasia, type 1c