| Gene Symbol |
NSUN5P2
|
| Entrez Gene |
260294
|
| Alt Symbol |
NOL1R2, NSUN5C, WBSCR20B, WBSCR20C
|
| Species |
Human
|
| Gene Type |
pseudo
|
| Description |
NOP2/Sun domain family, member 5 pseudogene 2
|
| Other Description |
NOL1/NOP2/Sun domain family, member 5C|NOP2/Sun domain family, member 5C (pseudogene)|Williams Beuren syndrome chromosome region 20C
|
| Swissprots |
Q63ZY6 A8K7U2 Q3KQU7 Q658S2 Q6NZ66 Q6PHS1 Q8N727 Q9HAH4
|
| Accessions |
Q63ZY6 AF416611 AAM62319 AF420250 AAL16068 AK021688 BAB13875 AK292107 BAF84796 AK303622 BAG64631 AK315927 BAH14298 AL117583 AL833016 CAH56289 BC007488 BC050591 BC056405 AAH56405 BC066297 BC082753 AAH82753 BC093976 AAH93976 BC101515 AAI01516 BC106049 AAI06050 BC107111 AAI07112 DA017627 NM_001039487 NM_148936 NM_148980 NR_033323
|
| Function |
May have S-adenosyl-L-methionine-dependent methyl- transferase activity. {ECO:0000305}.
|
| Tissue Specificity |
Ubiquitous. {ECO:0000269|PubMed:11978965, ECO:0000269|PubMed:12073013}.
|