Mmaa - methylmalonic aciduria (cobalamin deficiency) type A Gene
Also Known as 2810018E08Rik
Species: Mus musculus
Gene Type: protein coding
Gene ID: 109136
Summary
Predicted to enable several functions, including GTP binding activity; GTPase activity; and protein homodimerization activity. Predicted to be involved in cobalamin metabolic process. Predicted to be located in mitochondrion. Is expressed in several structures, including alimentary system; cardiovascular system; genitourinary system; lung; and trophectoderm. Human ortholog(s) of this gene implicated in methylmalonic acidemia cblA type. Orthologous to human MMAA (metabolism of cobalamin associated A). [provided by Alliance of Genome Resources, Apr 2022]
Mmaa Products (4)
| mRNA | Protein | Name |
|---|---|---|
| NM_001363470.1 | NP_001350399.1 | methylmalonic aciduria type A homolog, mitochondrial isoform a precursor |
| NM_001363471.1 | NP_001350400.1 | methylmalonic aciduria type A homolog, mitochondrial isoform b |
| NM_001363472.1 | NP_001350401.1 | methylmalonic aciduria type A homolog, mitochondrial isoform b |
| NM_133823.5 | NP_598584.2 | methylmalonic aciduria type A homolog, mitochondrial isoform a precursor |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
methylmalonic aciduria type A homolog, mitochondrial |
|
Related Agents
- Pre-clinical Phase
Pre-clinical Phase
Bioactive Molecules
(1)
| Cat. No. | Product Name |
Effect
|
Purity |
Rare Diseases
|
|---|---|---|---|---|
| HY-RS08507 | MMAA Human Pre-designed siRNA Set A | Pre-designed Set | / | Unkown |
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