Entity Details

Primary name TR13C_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ96RJ3
EntryNameTR13C_HUMAN
FullNameTumor necrosis factor receptor superfamily member 13C
TaxID9606
Evidenceevidence at protein level
Length184
SequenceStatuscomplete
DateCreated2002-05-27
DateModified2021-06-02

Ontological Relatives

GenesTNFRSF13C

GO terms

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GOName
GO:0002250 adaptive immune response
GO:0005886 plasma membrane
GO:0009897 external side of plasma membrane
GO:0016021 integral component of membrane
GO:0030890 positive regulation of B cell proliferation
GO:0031295 T cell costimulation
GO:0031296 B cell costimulation
GO:0033209 tumor necrosis factor-mediated signaling pathway
GO:0038023 signaling receptor activity
GO:0042102 positive regulation of T cell proliferation

Subcellular Location

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Subcellular Location
Membrane

Domains

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DomainNameCategoryType
IPR015336 Tumour necrosis factor receptor 13C, TALL-1 binding domainDomainDomain
IPR022338 Tumour necrosis factor receptor 13CFamilyFamily
IPR043521 Tumor necrosis factor receptor 13C/17FamilyFamily

Diseases

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Disease IDSourceNameDescription
613494 OMIMImmunodeficiency, common variable, 4 (CVID4)A primary immunodeficiency characterized by antibody deficiency, hypogammaglobulinemia, recurrent bacterial infections and an inability to mount an antibody response to antigen. The defect results from a failure of B-cell differentiation and impaired secretion of immunoglobulins; the numbers of circulating B-cells is usually in the normal range, but can be low. The disease is caused by variants affecting the gene represented in this entry.