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- Table of Contents
Facts about Probable 28S rRNA (cytosine-C(5))-methyltransferase.
Human | |
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Gene Name: | NSUN5 |
Uniprot: | Q96P11 |
Entrez: | 55695 |
Belongs to: |
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class I-like SAM-binding methyltransferase superfamily |
EC 2.1.1.-; FLJ10267; member 5A; MGC986; NOL1; NOL1/NOP2/Sun domain family member 5; NOL1/NOP2/Sun domain family, member 5; NOL1R(NOL1); NOL1-related protein; NOP2/Sun domain family, member 5; NSUN5A; p120; putative methyltransferase NSUN5; WBSCR20; WBSCR20A; Williams-Beuren syndrome chromosomal region 20A protein; Williams-Beuren syndrome critical region protein 20 copy A; Ynl022cL
Mass (kDA):
46.692 kDA
Human | |
---|---|
Location: | 7q11.23 |
Sequence: | 7; NC_000007.14 (73302516..73308867, complement) |
Ubiquitous. Detected in placenta, heart and skeletal muscle.
PMID: 11978965 by Doll A., et al. Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome.
PMID: 12073013 by Merla G., et al. Identification of additional transcripts in the Williams-Beuren syndrome critical region.