| Symbol: Name: ID: |
NSUN5 NOP2/Sun domain family, member 5 GFS:5500 |
| Gene name: | NSUN5 |
| Chromosome: | 7q11.23 |
| Previous Symbols: | WBSCR20, WBSCR20A |
| Previous Names: | Williams Beuren syndrome chromosome region 20A, "NOL1/NOP2/Sun domain family, member 5" |
| Aliases: | NOL1R, p120, (NOL1), FLJ10267, NSUN5A, Ynl022cL |
| Name Aliases: | NOP2/Sun domain family, member 5A |
| Locus Type: | gene with protein product |
| Mouse Genome Database ID: | MGI:2140844 | Rat Genome Database ID: | RGD:1309268 |
| HGNC ID: | HGNC:16385 | RefSeq IDs: | NM_001168347 |
| Entrez Gene ID: | 55695 | Ensembl Gene ID: | ENSG00000130305 |
| VEGA IDs: | OTTHUMG00000129869 | UniProt ID: | Q96P11 |
| UCSC ID: | uc003txv.2 | OMIM ID: | |
| Pubmed: | PMID11978965 PMID 12073013 | ||
| CCDS IDs: | CCDSCCDS5546.1 CCDS CCDS5547.1 | ||
Putative methyltransferase NSUN5 is an enzyme that in humans is encoded by the NSUN5 gene.
This gene encodes a member of the evolutionarily conserved NOL1/NOP2/Sun domain family. The encoded protein may function as a DNA methyltransferase in the nucleus. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2009].
Function: May have S-adenosyl-L-methionine-dependent methyl-transferase activity (Potential).
Products for NSUN5 gene
| Catalog | Product Name | Application | Company |
| GFS:E05500 | NOP2/Sun domain family, member 5; ELISA kit | ELISA | n/a |
| GFS:A05500 | NOP2/Sun domain family, member 5; Anti | ANTIBODIES | n/a |
| GFS:P05500 | NOP2/Sun domain family, member 5; Protien | Protien | n/a |
