XB-FEAT-958428: Difference between revisions
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=sept6= | =sept6= | ||
This is the community wiki page for the gene ''sept6'' 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 ''sept6'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase. | ||
=nomenclature changes= | |||
05.13.19 | |||
Human symbol has changed for genepage ID: 958428 From sept6 to SEPTIN6 | |||
Human symbol has changed for Entrez Gene: 23157. From SEPT6 to SEPTIN6 | |||
=Summary from NCBI for human = | |||
This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis. One version of pediatric acute myeloid leukemia is the result of a reciprocal translocation between chromosomes 11 and X, with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins. This gene encodes four transcript variants encoding three distinct isoforms. An additional transcript variant has been identified, but its biological validity has not been determined. [provided by RefSeq, Jul 2008] | |||
Latest revision as of 14:11, 21 May 2019
sept6
This is the community wiki page for the gene sept6 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
05.13.19
Human symbol has changed for genepage ID: 958428 From sept6 to SEPTIN6
Human symbol has changed for Entrez Gene: 23157. From SEPT6 to SEPTIN6
Summary from NCBI for human
This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis. One version of pediatric acute myeloid leukemia is the result of a reciprocal translocation between chromosomes 11 and X, with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins. This gene encodes four transcript variants encoding three distinct isoforms. An additional transcript variant has been identified, but its biological validity has not been determined. [provided by RefSeq, Jul 2008]