XB-FEAT-1003599: Difference between revisions
imported>Xenbase gene generator No edit summary |
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=top3a= | =top3a= | ||
This is the community wiki page for the gene ''top3a'' 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 ''top3a'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase. | ||
=nomenclature changes= | |||
08/07/2017 | |||
Human name has changed for Entrez Gene: 7156. From topoisomerase (DNA) III alpha to DNA topoisomerase III alpha | |||
=summary from NCBI= | |||
This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This enzyme catalyzes the transient breaking and rejoining of a single strand of DNA which allows the strands to pass through one another, thus reducing the number of supercoils and altering the topology of DNA. This enzyme forms a complex with BLM which functions in the regulation of recombination in somatic cells. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016] |
Latest revision as of 07:02, 8 August 2017
top3a
This is the community wiki page for the gene top3a please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
08/07/2017
Human name has changed for Entrez Gene: 7156. From topoisomerase (DNA) III alpha to DNA topoisomerase III alpha
summary from NCBI
This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This enzyme catalyzes the transient breaking and rejoining of a single strand of DNA which allows the strands to pass through one another, thus reducing the number of supercoils and altering the topology of DNA. This enzyme forms a complex with BLM which functions in the regulation of recombination in somatic cells. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]