Entity Details

Primary name TCO2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP20062
EntryNameTCO2_HUMAN
FullNameTranscobalamin-2
TaxID9606
Evidenceevidence at protein level
Length427
SequenceStatuscomplete
DateCreated1991-02-01
DateModified2021-06-02

Ontological Relatives

GenesTCN2

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

Subcellular Location

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Subcellular Location
Secreted

Domains

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DomainNameCategoryType
IPR002157 Cobalamin (vitamin B12)-binding proteinFamilyFamily
IPR008930 Terpenoid cyclases/protein prenyltransferase alpha-alpha toroidFamilyHomologous superfamily
IPR027954 Domain of unknown function DUF4430DomainDomain

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.

Drugs

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DrugNameSourceType
DB00115 CyanocobalaminDrugbanksmall molecule
DB00200 HydroxocobalaminDrugbanksmall molecule

Interactions

4 interactions