METT5D1 is a 407 amino acid protein that is thought to function as an S-adenosyl-L-methionine-dependent methyltransferase. Existing as four alternatively spliced isoforms, METT5D1 belongs to the RsmH family and methyltransferase superfamily. The gene encoding METT5D1 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Function:
Probable S-adenosyl-L-methionine-dependent methyltransferase.
Similarity:
Belongs to the methyltransferase superfamily. RsmH family.
SWISS:
A6NJ78
Gene ID:
196074
Database links:
Entrez Gene: 196074 Human
SwissProt: A6NJ78 Human
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