XB-FEAT-5954839: Difference between revisions
imported>Xenbase gene generator No edit summary |
imported>Xenbase |
||
| (3 intermediate revisions by the same user not shown) | |||
| Line 1: | Line 1: | ||
=utp14a= | =utp14a= | ||
This is the community wiki page for the gene ''utp14a'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | This is the community wiki page for the gene ''utp14a'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=nomenclature changes= | |||
05/29/2017 | |||
Human name has changed for Entrez Gene: 10813. From UTP14A small subunit processome component to UTP14A, small subunit processome component | |||
(added a comma) | |||
=summary= | |||
This gene encodes a member of the uridine triphosphate 14 family. As an essential component of a large ribonucleoprotein complex bound to the U3 small nucleolar RNA, the encoded protein is involved in ribosome biogenesis and 18S rRNA synthesis. In humans, an autosomal retrotransposed copy of this X-linked gene exists on chromosome 13. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009] | |||
Latest revision as of 08:57, 31 May 2017
utp14a
This is the community wiki page for the gene utp14a please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
05/29/2017 Human name has changed for Entrez Gene: 10813. From UTP14A small subunit processome component to UTP14A, small subunit processome component (added a comma)
summary
This gene encodes a member of the uridine triphosphate 14 family. As an essential component of a large ribonucleoprotein complex bound to the U3 small nucleolar RNA, the encoded protein is involved in ribosome biogenesis and 18S rRNA synthesis. In humans, an autosomal retrotransposed copy of this X-linked gene exists on chromosome 13. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]