Entity Details

Primary name TANGO2
Entity type gene
Source Source Link

Details

PrimaryID128989
RefseqGeneNG_046857
SymbolTANGO2
Nametransport and golgi organization 2 homolog
Chromosome22
Location22q11.21
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-11-30
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsTNG2_HUMAN

GO terms

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GOName
GO:0005794 Golgi apparatus
GO:0007030 Golgi organization
GO:0009306 protein secretion

Diseases

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Disease IDSourceNameDescription
616878 OMIMMetabolic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration (MECRCN)An autosomal recessive disorder characterized by metabolic encephalomyopathic crises, hypoglycemia, hyperammonemia, episodic rhabdomyolysis, susceptibility to life-threatening cardiac tachyarrhythmias, developmental delay, mental retardation, and mild diffuse cerebral atrophy. The disease is caused by variants affecting the gene represented in this entry.