XB-FEAT-5852281: Difference between revisions
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Note X. laevis has a duplication of this gene compared with Human- gene 1 is polr1d.1 and gene 2 is polr1d.2 | Note X. laevis has a duplication of this gene compared with Human- gene 1 is polr1d.1 and gene 2 is polr1d.2 | ||
=Summary from NCBI= | |||
The protein encoded by this gene is a component of the RNA polymerase I and RNA polymerase III complexes, which function in the synthesis of ribosomal RNA precursors and small RNAs, respectively. Mutations in this gene are a cause of Treacher Collins syndrome (TCS), a craniofacial development disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2011] | |||
Latest revision as of 06:30, 14 March 2018
polr1d.2
This is the community wiki page for the gene polr1d.2 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
03.12.18 Human name has changed for Entrez Gene: 51082. From RNA polymerase I subunit D to RNA polymerase I and III subunit D
Note X. laevis has a duplication of this gene compared with Human- gene 1 is polr1d.1 and gene 2 is polr1d.2
Summary from NCBI
The protein encoded by this gene is a component of the RNA polymerase I and RNA polymerase III complexes, which function in the synthesis of ribosomal RNA precursors and small RNAs, respectively. Mutations in this gene are a cause of Treacher Collins syndrome (TCS), a craniofacial development disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2011]