XB-FEAT-5954839: Difference between revisions

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Human name has changed for Entrez Gene: 10813. From UTP14A small subunit processome component to UTP14A, small subunit processome component
Human name has changed for Entrez Gene: 10813. From UTP14A small subunit processome component to UTP14A, small subunit processome component
(added a comma)
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=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. 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]
=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]