MMAA
<templatestyles src="Module:Hatnote/styles.css"></templatestyles>
Lua error in Module:Infobox_gene at line 33: attempt to index field 'wikibase' (a nil value).
Methylmalonic aciduria type A protein, mitochondrial also known as MMAA is a protein that in humans is encoded by the MMAA gene.[1]
Function
The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase.[2]
Clinical significance
Mutations in the MMAA gene are associated with methylmalonic acidemia.[1][3]
References
<templatestyles src="Reflist/styles.css" />
Cite error: Invalid <references> tag; parameter "group" is allowed only.
<references />, or <references group="..." />External links
Further reading
- Lua error in package.lua at line 80: module 'strict' not found.
- Lua error in package.lua at line 80: module 'strict' not found.
- Lua error in package.lua at line 80: module 'strict' not found.
- Lua error in package.lua at line 80: module 'strict' not found.
- Lua error in package.lua at line 80: module 'strict' not found.
- Lua error in package.lua at line 80: module 'strict' not found.
- Lua error in package.lua at line 80: module 'strict' not found.
- Lua error in package.lua at line 80: module 'strict' not found.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
<templatestyles src="Asbox/styles.css"></templatestyles>
 |
This article on a gene on human chromosome 4 is a stub. You can help Wikipedia by expanding it. |
