XB-FEAT-5795058: Difference between revisions
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imported>Xenbase →loc733352: Updated nomenclature, replaced: unnamed → loc733352 (2) |
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= | =''ccdc115''= | ||
This is the community wiki page for the gene '' | This is the community wiki page for the gene ''ccdc115'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=nomenclature changes= | |||
24APRIL2023 | |||
''Xenopus'' gene name updated from ''XB5795058 to ccdc115'' | |||
=Summary for human CCDC115 from NCBI= | |||
The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) vesicles in some human cells. The encoded protein shares some homology with the yeast V-ATPase assembly factor Vma22p, and the orthologous protein in mouse promotes cell proliferation and suppresses cell death. Defects in this gene are a cause of congenital disorder of glycosylation, type IIo in humans. [provided by RefSeq, Mar 2016] | |||
Latest revision as of 12:02, 24 April 2023
ccdc115
This is the community wiki page for the gene ccdc115 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
24APRIL2023
Xenopus gene name updated from XB5795058 to ccdc115
Summary for human CCDC115 from NCBI
The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) vesicles in some human cells. The encoded protein shares some homology with the yeast V-ATPase assembly factor Vma22p, and the orthologous protein in mouse promotes cell proliferation and suppresses cell death. Defects in this gene are a cause of congenital disorder of glycosylation, type IIo in humans. [provided by RefSeq, Mar 2016]