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
14 Pathways
- Post-translational protein modification,
- Post-translational protein phosphorylation,
- Metal ion SLC transporters,
- Transport of small molecules,
- Defective CP causes aceruloplasminemia (ACERULOP),
- Metabolism of proteins,
- Transport of bile salts and organic acids, metal ions and amine compounds,
- SLC-mediated transmembrane transport,
- Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs),
- Defective SLC40A1 causes hemochromatosis 4 (HFE4) (macrophages),
- Disorders of transmembrane transporters,
- SLC transporter disorders,
- Iron uptake and transport,
- 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
14 Pathways
- Post-translational protein modification,
- Post-translational protein phosphorylation,
- Metal ion SLC transporters,
- Transport of small molecules,
- Defective CP causes aceruloplasminemia (ACERULOP),
- Metabolism of proteins,
- Transport of bile salts and organic acids, metal ions and amine compounds,
- SLC-mediated transmembrane transport,
- Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs),
- Defective SLC40A1 causes hemochromatosis 4 (HFE4) (macrophages),
- Disorders of transmembrane transporters,
- SLC transporter disorders,
- Iron uptake and transport,
- Disease
