XB-FEAT-479246: Difference between revisions
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=foxd4l1.1= | =foxd4l1.1= | ||
This is the community wiki page for the gene ''foxd4l1.1'' 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 ''foxd4l1.1'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=nomenclature changes= | |||
06/19/2017 | |||
Human name has changed for Entrez Gene: 200350. From forkhead box D4-like 1 to forkhead box D4 like 1 (removed hyphen). | |||
=Note= | |||
There are 2 Xenopus homeologs for Human FOXD4L1, foxd4l1.1 and foxd4l1.2, | |||
=Summary from NCBI= | |||
This gene is a member of the forkhead/winged-helix (FOX) family of transcription factors with highly conserved FOX DNA-binding domains. Members of the FOX family of transcription factors are regulators of embryogenesis and may play a role in human cancer. This gene lies in a region of chromosome 2 that surrounds the site where two ancestral chromosomes fused to form human chromosome 2. This region is duplicated elsewhere in the human genome, primarily in subtelomeric and pericentromeric locations, thus mutiple copies of this gene have been found. [provided by RefSeq, Jul 2008] | |||
Latest revision as of 09:51, 20 June 2017
foxd4l1.1
This is the community wiki page for the gene foxd4l1.1 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
06/19/2017 Human name has changed for Entrez Gene: 200350. From forkhead box D4-like 1 to forkhead box D4 like 1 (removed hyphen).
Note
There are 2 Xenopus homeologs for Human FOXD4L1, foxd4l1.1 and foxd4l1.2,
Summary from NCBI
This gene is a member of the forkhead/winged-helix (FOX) family of transcription factors with highly conserved FOX DNA-binding domains. Members of the FOX family of transcription factors are regulators of embryogenesis and may play a role in human cancer. This gene lies in a region of chromosome 2 that surrounds the site where two ancestral chromosomes fused to form human chromosome 2. This region is duplicated elsewhere in the human genome, primarily in subtelomeric and pericentromeric locations, thus mutiple copies of this gene have been found. [provided by RefSeq, Jul 2008]