Homo sapiens Gene: TRAPPC2 | |||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Summary | |||||||||||||||||||||||
InnateDB Gene | IDBG-44932.6 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | TRAPPC2 | ||||||||||||||||||||||
Gene Name | trafficking protein particle complex 2 | ||||||||||||||||||||||
Synonyms | |||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Gene | ENSG00000196459 | ||||||||||||||||||||||
Encoded Proteins |
trafficking protein particle complex 2
trafficking protein particle complex 2
trafficking protein particle complex 2
trafficking protein particle complex 2
trafficking protein particle complex 2
|
||||||||||||||||||||||
Protein Structure | |||||||||||||||||||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||||||
Entrez Gene | |||||||||||||||||||||||
Summary |
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] |
||||||||||||||||||||||
Gene Information | |||||||||||||||||||||||
Type | Protein coding | ||||||||||||||||||||||
Genomic Location | Chromosome X:13712244-13734635 | ||||||||||||||||||||||
Strand | Reverse strand | ||||||||||||||||||||||
Band | p22.2 | ||||||||||||||||||||||
Transcripts | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 26 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
|
||||||||||||||||||||||
Gene Ontology | |||||||||||||||||||||||
Molecular Function |
|
||||||||||||||||||||||
Biological Process |
|
||||||||||||||||||||||
Cellular Component |
|
||||||||||||||||||||||
Orthologs | |||||||||||||||||||||||
Species
Mus musculus
|
Gene ID
Gene Order
|
||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | P0DI81 | ||||||||||||||||||||||
TrEMBL | E5RFG0 Q6IBE5 | ||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 6399 | ||||||||||||||||||||||
UniGene | Hs.592238 Hs.622292 Hs.630805 Hs.634785 | ||||||||||||||||||||||
RefSeq | NM_001128835 NM_001011658 NM_014563 | ||||||||||||||||||||||
HUGO | HGNC:23068 | ||||||||||||||||||||||
OMIM | 300202 | ||||||||||||||||||||||
CCDS | CCDS48083 CCDS48082 | ||||||||||||||||||||||
HPRD | 02189 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AC003002 AC003037 AF058918 AF157062 AF157063 AF157064 AF157065 AF291676 AK310542 AK313736 BC008889 BC016915 BC032809 BC052618 CH471074 CH471135 CR456859 DA542477 DB101396 | ||||||||||||||||||||||
GenPept | AAB80684 AAC14421 AAD49845 AAG02469 AAH16915 AAH52618 BAG36477 CAG33140 EAW72495 EAW72496 EAW98829 EAW98830 EAW98831 EAW98832 EAW98834 | ||||||||||||||||||||||
RNA Seq Atlas | 6399 | ||||||||||||||||||||||