XB-FEAT-5858238: Difference between revisions
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This is the community wiki page for the gene '' | This is the community wiki page for the gene ''peds1'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase. | ||
=nomenclature changes= | |||
2020/06/04 | |||
Human symbol has changed for Entrez Gene: 387521. From TMEM189 to PEDS1 | |||
Human and Xenopus name has changed for Entrez Gene: 387521. From transmembrane protein 189 to plasmanylethanolamine desaturase 1 | |||
Xenopus symbol has changed for genepage ID: 5858238 From tmem189 to ''peds1'' | |||
=SUMMARY FOR HUMAN PEDS1 FROM NCBI= | |||
Co-transcription of this gene and the neighboring downstream gene (ubiquitin-conjugating enzyme E2 variant 1) generates a rare read-through transcript, which encodes a fusion protein comprised of sequence sharing identity with each individual gene product. The protein encoded by this individual gene lacks a UEV1 domain but includes three transmembrane regions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2009]. | |||
Latest revision as of 06:47, 30 June 2020
peds1
This is the community wiki page for the gene peds1 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
2020/06/04 Human symbol has changed for Entrez Gene: 387521. From TMEM189 to PEDS1
Human and Xenopus name has changed for Entrez Gene: 387521. From transmembrane protein 189 to plasmanylethanolamine desaturase 1
Xenopus symbol has changed for genepage ID: 5858238 From tmem189 to peds1
SUMMARY FOR HUMAN PEDS1 FROM NCBI
Co-transcription of this gene and the neighboring downstream gene (ubiquitin-conjugating enzyme E2 variant 1) generates a rare read-through transcript, which encodes a fusion protein comprised of sequence sharing identity with each individual gene product. The protein encoded by this individual gene lacks a UEV1 domain but includes three transmembrane regions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2009].