XB-FEAT-1001222: Difference between revisions
imported>Xenbase →polr1d.1: Updated nomenclature, replaced: unnamed → polr1d.1 (2) |
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=polr1d | =''polr1d''= | ||
This is the community wiki page for the gene ''polr1d.1'' 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 ''polr1d.1'' 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 | |||
09.26.2024 | |||
''Xenopus'' gene symbol changed from ''polr1d.1'' to ''polr1d'' | |||
=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 11:18, 26 September 2024
polr1d
This is the community wiki page for the gene polr1d.1 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
09.26.2024
Xenopus gene symbol changed from polr1d.1 to polr1d
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]