node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
Mmaa | Mmab | ENSRNOP00000015508 | ENSRNOP00000066021 | Methylmalonic aciduria (Cobalamin deficiency) cblA type (Predicted), isoform CRA_a. | Corrinoid adenosyltransferase; Belongs to the Cob(I)alamin adenosyltransferase family. | 0.852 |
Mmaa | Mmachc | ENSRNOP00000015508 | ENSRNOP00000023178 | Methylmalonic aciduria (Cobalamin deficiency) cblA type (Predicted), isoform CRA_a. | Methylmalonic aciduria (Cobalamin deficiency) cblC type, with homocystinuria (Predicted). | 0.796 |
Mmaa | Mmadhc | ENSRNOP00000015508 | ENSRNOP00000058814 | Methylmalonic aciduria (Cobalamin deficiency) cblA type (Predicted), isoform CRA_a. | Methylmalonic aciduria and homocystinuria type D homolog, mitochondrial; Involved in cobalamin metabolism. Plays a role in regulating the biosynthesis of two coenzymes, methylcobalamin and adenosylcobalamin. Plays a role in regulating the proportion of methylcobalamin and adenosylcobalamin. Promotes oxidation of cob(II)alamin bound to MMACHC. | 0.831 |
Mmaa | Mtrr | ENSRNOP00000015508 | ENSRNOP00000024041 | Methylmalonic aciduria (Cobalamin deficiency) cblA type (Predicted), isoform CRA_a. | Methionine synthase reductase; Involved in the reductive regeneration of cob(I)alamin (vitamin B12) cofactor required for the maintenance of methionine synthase in a functional state. Necessary for utilization of methylgroups from the folate cycle, thereby affecting transgenerational epigenetic inheritance. Folate pathway donates methyl groups necessary for cellular methylation and affects different pathways such as DNA methylation, possibly explaining the transgenerational epigenetic inheritance effects. | 0.514 |
Mmab | Mmaa | ENSRNOP00000066021 | ENSRNOP00000015508 | Corrinoid adenosyltransferase; Belongs to the Cob(I)alamin adenosyltransferase family. | Methylmalonic aciduria (Cobalamin deficiency) cblA type (Predicted), isoform CRA_a. | 0.852 |
Mmab | Mmachc | ENSRNOP00000066021 | ENSRNOP00000023178 | Corrinoid adenosyltransferase; Belongs to the Cob(I)alamin adenosyltransferase family. | Methylmalonic aciduria (Cobalamin deficiency) cblC type, with homocystinuria (Predicted). | 0.718 |
Mmab | Mmadhc | ENSRNOP00000066021 | ENSRNOP00000058814 | Corrinoid adenosyltransferase; Belongs to the Cob(I)alamin adenosyltransferase family. | Methylmalonic aciduria and homocystinuria type D homolog, mitochondrial; Involved in cobalamin metabolism. Plays a role in regulating the biosynthesis of two coenzymes, methylcobalamin and adenosylcobalamin. Plays a role in regulating the proportion of methylcobalamin and adenosylcobalamin. Promotes oxidation of cob(II)alamin bound to MMACHC. | 0.841 |
Mmab | Mtrr | ENSRNOP00000066021 | ENSRNOP00000024041 | Corrinoid adenosyltransferase; Belongs to the Cob(I)alamin adenosyltransferase family. | Methionine synthase reductase; Involved in the reductive regeneration of cob(I)alamin (vitamin B12) cofactor required for the maintenance of methionine synthase in a functional state. Necessary for utilization of methylgroups from the folate cycle, thereby affecting transgenerational epigenetic inheritance. Folate pathway donates methyl groups necessary for cellular methylation and affects different pathways such as DNA methylation, possibly explaining the transgenerational epigenetic inheritance effects. | 0.504 |
Mmachc | Mmaa | ENSRNOP00000023178 | ENSRNOP00000015508 | Methylmalonic aciduria (Cobalamin deficiency) cblC type, with homocystinuria (Predicted). | Methylmalonic aciduria (Cobalamin deficiency) cblA type (Predicted), isoform CRA_a. | 0.796 |
Mmachc | Mmab | ENSRNOP00000023178 | ENSRNOP00000066021 | Methylmalonic aciduria (Cobalamin deficiency) cblC type, with homocystinuria (Predicted). | Corrinoid adenosyltransferase; Belongs to the Cob(I)alamin adenosyltransferase family. | 0.718 |
Mmachc | Mmadhc | ENSRNOP00000023178 | ENSRNOP00000058814 | Methylmalonic aciduria (Cobalamin deficiency) cblC type, with homocystinuria (Predicted). | Methylmalonic aciduria and homocystinuria type D homolog, mitochondrial; Involved in cobalamin metabolism. Plays a role in regulating the biosynthesis of two coenzymes, methylcobalamin and adenosylcobalamin. Plays a role in regulating the proportion of methylcobalamin and adenosylcobalamin. Promotes oxidation of cob(II)alamin bound to MMACHC. | 0.950 |
Mmachc | Mtrr | ENSRNOP00000023178 | ENSRNOP00000024041 | Methylmalonic aciduria (Cobalamin deficiency) cblC type, with homocystinuria (Predicted). | Methionine synthase reductase; Involved in the reductive regeneration of cob(I)alamin (vitamin B12) cofactor required for the maintenance of methionine synthase in a functional state. Necessary for utilization of methylgroups from the folate cycle, thereby affecting transgenerational epigenetic inheritance. Folate pathway donates methyl groups necessary for cellular methylation and affects different pathways such as DNA methylation, possibly explaining the transgenerational epigenetic inheritance effects. | 0.845 |
Mmadhc | Mmaa | ENSRNOP00000058814 | ENSRNOP00000015508 | Methylmalonic aciduria and homocystinuria type D homolog, mitochondrial; Involved in cobalamin metabolism. Plays a role in regulating the biosynthesis of two coenzymes, methylcobalamin and adenosylcobalamin. Plays a role in regulating the proportion of methylcobalamin and adenosylcobalamin. Promotes oxidation of cob(II)alamin bound to MMACHC. | Methylmalonic aciduria (Cobalamin deficiency) cblA type (Predicted), isoform CRA_a. | 0.831 |
Mmadhc | Mmab | ENSRNOP00000058814 | ENSRNOP00000066021 | Methylmalonic aciduria and homocystinuria type D homolog, mitochondrial; Involved in cobalamin metabolism. Plays a role in regulating the biosynthesis of two coenzymes, methylcobalamin and adenosylcobalamin. Plays a role in regulating the proportion of methylcobalamin and adenosylcobalamin. Promotes oxidation of cob(II)alamin bound to MMACHC. | Corrinoid adenosyltransferase; Belongs to the Cob(I)alamin adenosyltransferase family. | 0.841 |
Mmadhc | Mmachc | ENSRNOP00000058814 | ENSRNOP00000023178 | Methylmalonic aciduria and homocystinuria type D homolog, mitochondrial; Involved in cobalamin metabolism. Plays a role in regulating the biosynthesis of two coenzymes, methylcobalamin and adenosylcobalamin. Plays a role in regulating the proportion of methylcobalamin and adenosylcobalamin. Promotes oxidation of cob(II)alamin bound to MMACHC. | Methylmalonic aciduria (Cobalamin deficiency) cblC type, with homocystinuria (Predicted). | 0.950 |
Mmadhc | Mtrr | ENSRNOP00000058814 | ENSRNOP00000024041 | Methylmalonic aciduria and homocystinuria type D homolog, mitochondrial; Involved in cobalamin metabolism. Plays a role in regulating the biosynthesis of two coenzymes, methylcobalamin and adenosylcobalamin. Plays a role in regulating the proportion of methylcobalamin and adenosylcobalamin. Promotes oxidation of cob(II)alamin bound to MMACHC. | Methionine synthase reductase; Involved in the reductive regeneration of cob(I)alamin (vitamin B12) cofactor required for the maintenance of methionine synthase in a functional state. Necessary for utilization of methylgroups from the folate cycle, thereby affecting transgenerational epigenetic inheritance. Folate pathway donates methyl groups necessary for cellular methylation and affects different pathways such as DNA methylation, possibly explaining the transgenerational epigenetic inheritance effects. | 0.858 |
Mtrr | Mmaa | ENSRNOP00000024041 | ENSRNOP00000015508 | Methionine synthase reductase; Involved in the reductive regeneration of cob(I)alamin (vitamin B12) cofactor required for the maintenance of methionine synthase in a functional state. Necessary for utilization of methylgroups from the folate cycle, thereby affecting transgenerational epigenetic inheritance. Folate pathway donates methyl groups necessary for cellular methylation and affects different pathways such as DNA methylation, possibly explaining the transgenerational epigenetic inheritance effects. | Methylmalonic aciduria (Cobalamin deficiency) cblA type (Predicted), isoform CRA_a. | 0.514 |
Mtrr | Mmab | ENSRNOP00000024041 | ENSRNOP00000066021 | Methionine synthase reductase; Involved in the reductive regeneration of cob(I)alamin (vitamin B12) cofactor required for the maintenance of methionine synthase in a functional state. Necessary for utilization of methylgroups from the folate cycle, thereby affecting transgenerational epigenetic inheritance. Folate pathway donates methyl groups necessary for cellular methylation and affects different pathways such as DNA methylation, possibly explaining the transgenerational epigenetic inheritance effects. | Corrinoid adenosyltransferase; Belongs to the Cob(I)alamin adenosyltransferase family. | 0.504 |
Mtrr | Mmachc | ENSRNOP00000024041 | ENSRNOP00000023178 | Methionine synthase reductase; Involved in the reductive regeneration of cob(I)alamin (vitamin B12) cofactor required for the maintenance of methionine synthase in a functional state. Necessary for utilization of methylgroups from the folate cycle, thereby affecting transgenerational epigenetic inheritance. Folate pathway donates methyl groups necessary for cellular methylation and affects different pathways such as DNA methylation, possibly explaining the transgenerational epigenetic inheritance effects. | Methylmalonic aciduria (Cobalamin deficiency) cblC type, with homocystinuria (Predicted). | 0.845 |
Mtrr | Mmadhc | ENSRNOP00000024041 | ENSRNOP00000058814 | Methionine synthase reductase; Involved in the reductive regeneration of cob(I)alamin (vitamin B12) cofactor required for the maintenance of methionine synthase in a functional state. Necessary for utilization of methylgroups from the folate cycle, thereby affecting transgenerational epigenetic inheritance. Folate pathway donates methyl groups necessary for cellular methylation and affects different pathways such as DNA methylation, possibly explaining the transgenerational epigenetic inheritance effects. | Methylmalonic aciduria and homocystinuria type D homolog, mitochondrial; Involved in cobalamin metabolism. Plays a role in regulating the biosynthesis of two coenzymes, methylcobalamin and adenosylcobalamin. Plays a role in regulating the proportion of methylcobalamin and adenosylcobalamin. Promotes oxidation of cob(II)alamin bound to MMACHC. | 0.858 |