Entity Details

Primary name TCN2
Entity type gene
Source Source Link

Details

PrimaryID6948
RefseqGeneNG_007263
SymbolTCN2
Nametranscobalamin 2
Chromosome22
Location22q12.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-08-18
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsTCO2_HUMAN

GO terms

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GOName
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005768 endosome
GO:0006824 cobalt ion transport
GO:0009235 cobalamin metabolic process
GO:0015889 cobalamin transport
GO:0031419 cobalamin binding
GO:0043202 lysosomal lumen
GO:0046872 metal ion binding

Diseases

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Disease IDSourceNameDescription
275350 OMIMTranscobalamin II deficiency (TCN2 deficiency)Results in various forms of anemia. The disease is caused by variants affecting the gene represented in this entry.

Interactions

5 interactions

InteractorPartnerSourcesPublicationsLink
TCN2PAXIP1BioGRID, IntAct21163940 details
TCN2CBLBioGRID11788601 details
TCN2APPBioGRID21832049 details
TCN2RHOUBioGRID26598620 details
TCN2LIPFBioGRID26186194 details