XB-FEAT-965016: Difference between revisions
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=trappc2= | =trappc2= | ||
This is the community wiki page for the gene ''trappc2'' 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 ''trappc2'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=nomenclature changes = | |||
02.17.2021 | |||
Human name has changed for Entrez Gene: 6399. From trafficking protein particle complex 2 to trafficking protein particle complex subunit 2 | |||
=summary for human TRAPPC2 from NCBI= | |||
The protein encoded by this gene is thought to be part of a large multi-subunit complex involved in the targeting and fusion of endoplasmic reticulum-to-Golgi transport vesicles with their acceptor compartment. In addition, the encoded protein can bind c-myc promoter-binding protein 1 and block its transcriptional repression capability. Mutations in this gene are a cause of spondyloepiphyseal dysplasia tarda (SEDT). A processed pseudogene of this gene is located on chromosome 19, and other pseudogenes are found on chromosomes 8 and Y. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010] | |||
Latest revision as of 14:59, 19 February 2021
trappc2
This is the community wiki page for the gene trappc2 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
02.17.2021 Human name has changed for Entrez Gene: 6399. From trafficking protein particle complex 2 to trafficking protein particle complex subunit 2
summary for human TRAPPC2 from NCBI
The protein encoded by this gene is thought to be part of a large multi-subunit complex involved in the targeting and fusion of endoplasmic reticulum-to-Golgi transport vesicles with their acceptor compartment. In addition, the encoded protein can bind c-myc promoter-binding protein 1 and block its transcriptional repression capability. Mutations in this gene are a cause of spondyloepiphyseal dysplasia tarda (SEDT). A processed pseudogene of this gene is located on chromosome 19, and other pseudogenes are found on chromosomes 8 and Y. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010]