The phenotype associated with variants in TANGO2 may be explained by a dual role of the protein in ER‐to‐Golgi transport and at the mitochondria

Homozygous TANGO2 Single Nucleotide Variants Presenting with Additional Manifestations Resembling Alternating Hemiplegia of Childhood–Expanding the Phenotype of a Recently Reported Condition

(2019) Melissa Hicks et al.   NEUROPEDIATRICS

TANGO2 deficiency as a cause of neurodevelopmental delay with indirect effects on mitochondrial energy metabolism

(2019) Elizabeth Jennions et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Clinical presentation and proteomic signature of patients with TANGO2 mutations

(2019) Mingirulli Nadja et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Characterization of three TRAPPC11 variants suggests a critical role for the extreme carboxy terminus of the protein

(2019) Miroslav P. Milev et al.   Scientific Reports

TANGO2: expanding the clinical phenotype and spectrum of pathogenic variants

(2018) Jennifer N. Dines et al.   GENETICS IN MEDICINE

Bi-allelic mutations inTRAPPC2Lresult in a neurodevelopmental disorder and have an impact on RAB11 in fibroblasts

(2018) Miroslav P Milev et al.   JOURNAL OF MEDICAL GENETICS

Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations

(2016) Seema R. Lalani et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy

(2016) Laura S. Kremer et al.   AMERICAN JOURNAL OF HUMAN GENETICS

MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins

(2015) Sarah E. Calvo et al.   NUCLEIC ACIDS RESEARCH

Synchronization of secretory protein traffic in populations of cells

(2012) Gaelle Boncompain et al.   NATURE METHODS

Reconstitution of Mitochondria Derived Vesicle Formation Demonstrates Selective Enrichment of Oxidized Cargo

(2012) Vincent Soubannier et al.   PLoS One

TANGO1 Facilitates Cargo Loading at Endoplasmic Reticulum Exit Sites

(2009) Kota Saito et al.   CELL

TRAPPC2L is a Novel, Highly Conserved TRAPP-Interacting Protein

(2009) P. James Scrivens et al.   TRAFFIC

Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes

(2008) T.M. Maynard et al.   MOLECULAR AND CELLULAR NEUROSCIENCE

The TRAPP Complex: Insights into its Architecture and Function

(2008) Michael Sacher et al.   TRAFFIC