Target intelligence / Profile preview

Trafficking protein particle complex subunit 10 (TRAPPC10)

Target
TRAPPC10
Molecular classification
Other, Membrane trafficking complex subunit, Vesicle tethering complex subunit
01

Overview

Trafficking protein particle complex subunit 10 (TRAPPC10) is a specific subunit of the transport protein particle (TRAPP) II complex, a conserved multisubunit tethering complex essential for vesicle-mediated trafficking in eukaryotic cells. TRAPPC10 is a transmembrane protein localized to the cis-Golgi network and functions primarily in late Golgi trafficking by acting as a membrane tether, facilitating vesicle docking and fusion events critical for ER-to-Golgi and intra-Golgi transport. It participates in the organization of the Golgi apparatus and is necessary for proper secretory pathway function. Multiple alternatively spliced mRNA variants exist, with possibly tissue-specific roles. Pathogenic variants in TRAPPC10 have been implicated in severe neurodevelopmental disorders, including microcephalic syndromes in humans and mice[1][2][3][4][5][6]. There are currently no characterized pharmacological inhibitors or drugs directly targeting TRAPPC10, and it is not a common direct therapeutic target.

Other names
EHOC1TMEM1EHOC-1TRAPP subunit TMEM1TRS130Epilepsy holoprosencephaly candidate 1 proteinProtein GT334Trafficking protein particle complex subunit TMEM1Transport protein particle subunit TMEM1Trafficking protein particle complex subunit 130TRAPP 130 kDa subunitGT334NEDMISSTRS30
02

Biological functions

Membrane traffickingVesicle-mediated transportER-to-Golgi traffickingGolgi apparatus organizationSecretory pathwayIntra-Golgi and endosome-to-Golgi transport
03

Disease associations

Neurodevelopmental disorder with microcephaly, short stature and speech delayPrimary autosomal recessive microcephalyProgressive myoclonus epilepsy (Unverricht-Lundborg type) (possible)Autoimmune polyglandular disease type 1 (possible)
04

Safety considerations

No direct safety concerns described, but loss of function or pathogenic variation can cause severe neurodevelopmental disorders and microcephaly

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