XB-FEAT-942471: Difference between revisions
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Human name has changed for Entrez Gene: 8468. From FK506 binding protein 6 to FKBP prolyl isomerase 6 | Human name has changed for Entrez Gene: 8468. From FK506 binding protein 6 to FKBP prolyl isomerase 6 | ||
10.15.2020 | |||
Human name has changed for Entrez Gene: 8468. From FKBP prolyl isomerase 6 to FKBP prolyl isomerase family member 6 (inactive) ( gene symbol unchanged) | |||
Xenopus name has changed for XB-GENEPAGE942471, from From FKBP prolyl isomerase 6 to FKBP prolyl isomerase family member | |||
Note: checking with HGNC to see if this gene is inactive in human and other vertebrates or just primates/humans. | |||
=summary for human FKBP6 from NCBI= | |||
The protein encoded by this gene is a cis-trans peptidyl-prolyl isomerase that may function in immunoregulation and basic cellular processes involving protein folding and trafficking. This gene is located in a chromosomal region that is deleted in Williams-Beuren syndrome. Defects in this gene may cause male infertility. There are multiple pseudogenes for this gene located nearby on chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013] | |||
Latest revision as of 12:28, 4 November 2020
fkbp6
This is the community wiki page for the gene fkbp6 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
Nomenclature updates
11/06/2018 Human name has changed for Entrez Gene: 8468. From FK506 binding protein 6 to FKBP prolyl isomerase 6
10.15.2020
Human name has changed for Entrez Gene: 8468. From FKBP prolyl isomerase 6 to FKBP prolyl isomerase family member 6 (inactive) ( gene symbol unchanged)
Xenopus name has changed for XB-GENEPAGE942471, from From FKBP prolyl isomerase 6 to FKBP prolyl isomerase family member
Note: checking with HGNC to see if this gene is inactive in human and other vertebrates or just primates/humans.
summary for human FKBP6 from NCBI
The protein encoded by this gene is a cis-trans peptidyl-prolyl isomerase that may function in immunoregulation and basic cellular processes involving protein folding and trafficking. This gene is located in a chromosomal region that is deleted in Williams-Beuren syndrome. Defects in this gene may cause male infertility. There are multiple pseudogenes for this gene located nearby on chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]