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Function
Gene Ontology Displayer
13 Pathways
- Cytochrome P450 - arranged by substrate type,
- Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA),
- Signal Transduction,
- RA biosynthesis pathway,
- Phase I - Functionalization of compounds,
- Disease,
- Diseases of metabolism,
- Metabolism,
- Vitamins,
- Signaling by Retinoic Acid,
- Signaling by Nuclear Receptors,
- Biological oxidations,
- Metabolic disorders of biological oxidation enzymes
Gene --> GO terms.
Gene -> HPO annotation (Human Phenotype Ontology)
Mouse Gene --> Allele [Phenotype]
Genomics
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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
13 Pathways
- Cytochrome P450 - arranged by substrate type,
- Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA),
- Signal Transduction,
- RA biosynthesis pathway,
- Phase I - Functionalization of compounds,
- Disease,
- Diseases of metabolism,
- Metabolism,
- Vitamins,
- Signaling by Retinoic Acid,
- Signaling by Nuclear Receptors,
- Biological oxidations,
- Metabolic disorders of biological oxidation enzymes