Uni Prot Comments Displayer
Protein Atlas Displayer
Gene Expression Atlas Tissues Displayer
Gene Expression Atlas Diseases Displayer
Publication Counts Displayer
Curated Proteins Displayer
Function
Gene Ontology Displayer
9 Pathways
- Defective B3GALTL causes Peters-plus syndrome (PpS),
- Metabolism of proteins,
- O-linked glycosylation,
- O-glycosylation of TSR domain-containing proteins,
- Post-translational protein modification,
- Diseases of glycosylation,
- Diseases associated with O-glycosylation of proteins,
- Diseases of metabolism,
- Disease
Gene --> GO terms.
Gene -> HPO annotation (Human Phenotype Ontology)
Mouse Gene --> Allele [Phenotype]
Genomics
J Browse Displayer
Gene Structure Displayer
Overlapping Features Displayer
Mouse Alleles Displayer
Gene --> Chromosomal location.
Gene --> GO terms.
Gene --> Overlapping genes.
Disease
Gene (Hum OR Rat) --> Mouse Allele (Phenotype)
Gene --> Alleles and Disease (clinVar data)
Gene -> HPO annotation (Human Phenotype Ontology)
Mouse Gene --> Allele [Phenotype]
Other
9 Pathways
- Defective B3GALTL causes Peters-plus syndrome (PpS),
- Metabolism of proteins,
- O-linked glycosylation,
- O-glycosylation of TSR domain-containing proteins,
- Post-translational protein modification,
- Diseases of glycosylation,
- Diseases associated with O-glycosylation of proteins,
- Diseases of metabolism,
- Disease
