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Curated Proteins Displayer
Function
Gene Ontology Displayer
19 Pathways
- Defects in vitamin and cofactor metabolism,
- Methylation,
- Phase II - Conjugation of compounds,
- Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE,
- Cysteine and methionine metabolism,
- Metabolism of water-soluble vitamins and cofactors,
- Metabolism,
- Diseases of metabolism,
- Selenocompound metabolism,
- Metabolism of amino acids and derivatives,
- Metabolic pathways,
- Metabolism of vitamins and cofactors,
- Biological oxidations,
- Cobalamin (Cbl, vitamin B12) transport and metabolism,
- One carbon pool by folate,
- Sulfur amino acid metabolism,
- Defective MTR causes methylmalonic aciduria and homocystinuria type cblG,
- Disease,
- Defects in cobalamin (B12) metabolism
Gene --> GO terms.
Gene -> HPO annotation (Human Phenotype Ontology)
Mouse Gene --> Allele [Phenotype]
Genomics
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Gene Structure Displayer
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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
19 Pathways
- Defects in vitamin and cofactor metabolism,
- Methylation,
- Phase II - Conjugation of compounds,
- Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE,
- Cysteine and methionine metabolism,
- Metabolism of water-soluble vitamins and cofactors,
- Metabolism,
- Diseases of metabolism,
- Selenocompound metabolism,
- Metabolism of amino acids and derivatives,
- Metabolic pathways,
- Metabolism of vitamins and cofactors,
- Biological oxidations,
- Cobalamin (Cbl, vitamin B12) transport and metabolism,
- One carbon pool by folate,
- Sulfur amino acid metabolism,
- Defective MTR causes methylmalonic aciduria and homocystinuria type cblG,
- Disease,
- Defects in cobalamin (B12) metabolism
