TNFRSF13C - TNF receptor superfamily member 13C Gene

Also Known as BAFFR; CD268; CVID4; BAFF-R; BROMIX; prolixin

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 115650

About TNFRSF13C

Cytogenetic location: 22q13.2 Genomic coordinates (GRCh38): 22:41,922,032-41,926,806 (from NCBI)

This gene has 1 transcript (splice variant), 91 orthologues, 1 paralogue and is associated with 3 phenotypes. Biased expression in spleen (RPKM 19.7), lymph node (RPKM 17.1) and 5 other tissues.

Summary

B cell-activating factor (BAFF) enhances B-cell survival in vitro and is a regulator of the peripheral B-cell population. Overexpression of Baff in mice results in mature B-cell hyperplasia and symptoms of systemic lupus erythematosus (SLE). Also, some SLE patients have increased levels of BAFF in serum. Therefore, it has been proposed that abnormally high levels of BAFF may contribute to the pathogenesis of autoimmune diseases by enhancing the survival of autoreactive B cells. The protein encoded by this gene is a receptor for BAFF and is a type III transmembrane protein containing a single extracellular cysteine-rich domain. It is thought that this receptor is the principal receptor required for BAFF-mediated mature B-cell survival. [provided by RefSeq, Jul 2008]

TNFRSF13C Products (1)

mRNA Protein Name
NM_052945.4 NP_443177.1 tumor necrosis factor receptor superfamily member 13C

TNFRSF13C Protein Structure

BaffR-Tall_bind

BaffR-Tall_bind: BAFF-R, TALL-1 binding (16 - 46)

  • 0
  • 100
  • 184 a.a.
Protein Preferred Names Protein Names

tumor necrosis factor receptor superfamily member 13C

  • B cell-activating factor receptor

Recombinant TNFRSF13C Proteins

Art. -Nr. Produktname Accession Reinheit
HY-P7130 BAFFR/TNFRSF13C Protein, Human Q96RJ3-1 (M1-G76) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P72764 BAFFR/TNFRSF13C Protein, Human (HEK293, His) Q96RJ3-1 (S7-A71) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P78065 BAFFR/TNFRSF13C Protein, Human (Biotinylated, HEK293, His-Avi) Q96RJ3-1 (S7-A71) ≥ 95%, as determined by Bis-Tris PAGE.
HY-P700453 BAFFR/TNFRSF13C Protein, Human (HEK293, hFc-Flag) Q96RJ3-1 (S7-A71) ≥ 95%, as determined by reducing SDS-PAGE.

TNFRSF13C Antibodies

Art. -Nr. Produktname Anwendung Reactivity
HY-P81611 BAFFR Antibody (YA1356) FC, ELISA Human
HY-P84740 BAFFR Antibody (YA4437) WB, FC, ELISA Human, Rat
HY-P84740A BAFFR Antibody (YA4437)(PBS only) WB, FC, ELISA Human, Rat

Related Diseases

Diseases Alias
Immunodeficiency, Common Variable, 4
  • CVID4

  • Antibody Deficiency Due To Baffr Defect

  • Common Variable Immunodeficiency 4

  • Immunodeficiency, Variable, Common, Type 4

Common Variable Immunodeficiency
  • Cvid

  • Common Variable Agammaglobulinemia

  • Common Variable Immune Deficiency

  • Acquired Hypogammaglobulinemia

  • Hypogamma-Globulinemia, Acquired

  • Idiopathic Immunoglobulin Deficiency

  • Primary Antibody Deficiency

  • Primary Hypogammaglobulinemia

  • Acquired Agammaglobulinemia

  • Sporadic Hypogammaglobulinemia

  • Common Variable Hypogamma-Globulinemia

  • Immunoglobulin Deficiency, Late-Onset

  • Common Variable Hypogammaglobulinemia

  • Immunodeficiency, Common Variable

Immunodeficiency, Common Variable, 2
  • CVID2

  • Antibody Deficiency Due To Taci Defect

  • Hypogammaglobulinemia Due To Taci Deficiency

  • Common Variable Immunodeficiency 2

  • Immunodeficiency, Variable, Common, Type 2

Primary Agammaglobulinemia
  • Immunoglobulin Deficiency

  • Antibody Deficiency Syndrome

  • Antibody

  • Antibody Deficiency

  • Gammaglobulin Deficiency

  • Antibody Deficiency With Near-Normal Immunoglobulins Or With Hyperimmunoglobulinaemia

  • Immunoglobulin Deficiency With Near-Normal Immunoglobins

  • Immunoglobulin Deficiency With Hyperimmunoglobulinaemia

  • Antibody Immunodeficiency With Hyperimmunoglobulinaemia

  • Antibody Deficiency With Hyperimmunoglobulinaemia

Lupus Erythematosus
  • Lupus

  • Lupus Vulgaris

  • Lupus Erythematosus, Discoid

  • Lupus Erythematosus, Systemic

  • Subacute Cutaneous Lupus

  • Le - [Lupus Erythematosus]

Autoimmune Disease
  • Autoimmune Diseases

  • Autoimmune Hypersensitivity Disease

  • Hypersensitivity Reaction Type Ii Disease

  • Type Ii Hypersensitivity Reaction Disease

Systemic Lupus Erythematosus
  • Lupus Nephritis

  • SLE

  • Disseminated Lupus Erythematosus

  • Systemic Lupus Erythematosus, Susceptibility To

  • Lupus Erythematosus, Systemic

  • Lupus Nephritis, Susceptibility To

  • Libman-Sacks Disease

  • Systemic Lupus Erythematosus Susceptibility To

  • Sle - Lupus Erythematosus, Systemic

  • Le Syndrome

  • Lupus

  • Lupus Erythematosus Systemic

  • Lupus Erythematosus, Systemic, Susceptibility To

  • Lupus Vulgaris

  • Lupus Erythematosus, Discoid

  • Lupus Erythematosus

  • Systemic Lupus Erythematosus Nos

  • Sle - [Systemic Lupus Erythematosus]

Follicular Lymphoma
  • Lymphoma, Follicular

  • Lymphoma Follicular

  • Brill-Symmers' Disease

  • Large Cell Follicular Non-Hodgkin Lymphoma

  • Diffuse Follicle Centre Lymphoma

  • Diffuse Follicular Lymphoma Nos

  • Follicular Nodular Non-Hodgkin Lymphoma, Unspecified

  • Follicular Large Cell Cleaved Or Noncleaved Lymphoma

  • Large Cell Follicular Noncleaved Lymphoma

  • Follicular Lymphoma With Or Without Diffuse Areas

  • Histiocytic Follicular Lymphoma

  • Histiocytic Nodular Lymphoma

  • Histiocytic Nodular Malignant Lymphoma

  • Large Cell Follicular Lymphoma

  • Large Cell Noncleaved Follicular Lymphoma

  • Large Cell Noncleaved Follicular Malignant Lymphoma

  • Nodular Reticulum Cell Sarcoma

  • Noncleaved Follicular Lymphoma

Macroglobulinemia
  • Primary Macroglobulinemia

  • Waldenstrom Macroglobulinemia

Transient Hypogammaglobulinemia Of Infancy
  • Immunoglobulin Maturational Delay

  • Thi - [Transient Hypogammaglobulinaemia Of Infancy]

B-Cell Lymphoma
  • Lymphoma, B-Cell

  • B-Cell Lymphomas

  • B-Cell Lymphocytic Neoplasm

  • Lymphoma B-Cell

  • B-Cell Lymphoma Nos

Cd40 Ligand Deficiency
  • X-Linked Hyper Igm Syndrome

  • Hyperimmunoglobulin M Syndrome

  • Higm1

  • Hyper-Igm Syndrome Type 1

  • X-Linked Hyper-Igm Syndrome

  • Xhigm

  • Higmx-1

  • X-Linked Hyper-Igm Immunodeficiency

  • Hyper-Igm Syndrome 1

  • Immunodeficiency With Hyper-Igm, Type 1

  • Hyper-Igm Syndrome Due To Cd40 Ligand Deficiency

  • Hyper-Igm Syndrome Due To Cd40l Deficiency

  • Hyper-Igm Immunodeficiency Syndrome

  • Hyper-Igm Immunodeficiency Syndrome, Type 1

Transient Hypogammaglobulinemia
Trypanosomiasis
B Cell Deficiency
  • Immunoglobulin Heavy Chain Deficiency

  • B Cell Deficiencies

  • Immunoglobulin Heavy Chain Deletion

  • Humoral Immune Defect

Selective Igg Deficiency Disease
  • Igg Deficiency

  • Immunoglobin G Subclass Deficiency

  • Selective Deficiency Of Igg

  • Selective Igg Immunodeficiency

  • Selective Immunoglobulin G Deficiency

  • Selective Immunoglobulin G Subclass Deficiency

Lymphoma, Non-Hodgkin, Familial
  • Non-Hodgkin Lymphoma

  • Lymphoma, Non-Hodgkin

  • NHL

  • Lymphoma, Non-Hodgkin, Somatic

  • Lymphoma, Follicular, Somatic

  • Familial Non-Hodgkin Lymphoma

  • Lymphoma Non-Hodgkins

  • Follicular Lymphoma, Somatic

  • Lymphosarcoma

  • Non-Hodgkins Lymphoma

Immunodeficiency With Hyper-Igm, Type 4
  • HIGM4

  • Hyper-Igm Syndrome Type 4

  • Immunodeficiency With Hyper-Igm Type 4

  • Hyper-Igm Syndrome 4

  • Immunodeficiency With Hyper Igm Type 4

  • Hyper Igm Syndrome 4

  • Immunodeficiency, With Hyper Igm, Type 4

Multiple Sclerosis
  • MS

  • Multiple Sclerosis, Susceptibility To

  • Disseminated Sclerosis

  • Multiple Sclerosis, Disease Progression, Modifier Of

  • Insular Sclerosis

  • Multiple Sclerosis Modifier Of Disease Progression

  • Multiple Sclerosis, Susceptibility To 1

  • Multiple Sclerosis, Susceptibility To, 1

  • Multiple Sclerosis 1

  • Generalized Multiple Sclerosis

  • Multiple Sclerosis Variant

  • Multiple Sclerosis Susceptibility To

  • Cerebrospinal Sclerosis

  • Generalised Multiple Sclerosis

  • Ms - [Multiple Sclerosis]

  • Disseminated Cerebrospinal Sclerosis

  • Disseminated Multiple Sclerosis

  • Disseminated Nervous System Myelosclerosis

  • Multiple Cerebrospinal Sclerosis

  • Multiple Combined Sclerosis

  • Multiple Sclerosis Generalised

  • Disseminated Brain Sclerosis

  • Disseminated Spinal Sclerosis

  • Insular Brain Sclerosis

  • Miliary Brain Sclerosis

  • Multiple Combined Sclerosis Of Spinal Cord

  • Multiple Ascending Sclerosis

  • Multiple Brain Sclerosis

  • Multiple Sclerosis Of Brain Stem

  • Multiple Sclerosis Of The Brain Stem

  • Multiple Sclerosis Of Cord

  • Sclérose En Plaques

  • Plaque Sclerosis

  • Multiple Sclerosis Of The Spinal Cord

Immunoglobulin Alpha Deficiency
  • Iga Deficiency

  • Gamma-A-Globulin Deficiency

  • Immunoglobulin A Deficiency

Potocki-Shaffer Syndrome
  • Proximal 11p Deletion Syndrome

  • Chromosome 11p11.2 Deletion Syndrome

  • Pss

  • 11p11.2 Deletion

  • P11pds

  • Defect11 Syndrome

  • Deletion Of Chromosome 11p11.2

  • POSHS

Immunodeficiency With Hyper-Igm, Type 3
  • HIGM3

  • Immunodeficiency With Hyper Igm Type 3

  • Hyper-Igm Syndrome Type 3

  • Hyper-Igm Syndrome 3

  • Hyper-Igm Syndrome Due To Cd40 Deficiency

  • Cd40 Deficiency

  • Type 3 Hyper-Igm Immunodeficiency

  • Hyper Igm Syndrome 3

  • Immunodeficiency With Hyper-Igm 3

  • Hyper-Igm Immunodeficiency Type 3

  • Immunodeficiency, With Hyper Igm, Type 3

  • Hyper-Igm Immunodeficiency Syndrome, Type 3

Immunodeficiency With Hyper-Igm, Type 1
  • Immunodeficiency, X-Linked, With Hyper-Igm

  • Hyper Igm Syndrome

  • HIGM1

  • Xhim

  • Hyper-Igm Syndrome

  • Higm

  • Hyper-Igm Syndrome 1

  • Immunodeficiency 3

  • Imd3

  • Immunodeficiency With Hyper-Igm

  • Immunodeficiency With Hyper Igm Type 1

  • Ihis

  • X-Linked Hyper Igm Syndrome

  • Hyper-Igm Immunodeficiency, X-Linked

  • Hyper Igm Immunodeficiency, X-Linked

  • Hyper Igm Syndrome 1

  • X-Linked Immunodeficiency With Hyper-Igm 1

  • Immunodeficiency, With Hyper Igm

  • Immunodeficiency, With Hyper Igm, Type 1

  • Hyper-Igm Immunodeficiency Syndrome, Type 1

  • Hyperimmunoglobulin M Syndrome

Good Syndrome
  • Immunodeficiency With Thymoma

  • Thymoma-Immunodeficiency Syndrome

  • Thymoma With Hypogammaglobulinemia

  • Thymoma Immunodeficiency

Rheumatoid Arthritis
  • RA

  • Arthritis, Rheumatoid

  • Rheumatoid Arthritis, Susceptibility To

  • Arthritis Or Polyarthritis, Rheumatic

  • Atrophic Arthritis

  • Rheumatism Arthritis

  • Rheumatoid Polyarthritis

Lymphoid Interstitial Pneumonia
  • Lymphocytic Interstitial Pneumonia

  • Lip Disease

  • Lip Diseases

  • LIP

  • Disease Of Lips

Autoimmune Disease Of Exocrine System
Leukemia, Chronic Lymphocytic
  • Chronic Lymphocytic Leukemia

  • B-Cell Chronic Lymphocytic Leukemia

  • CLL

  • B-Cell Chronic Lymphoid Leukemia

  • Chronic Lymphatic Leukemia

  • Chronic Lymphocytic Leukaemia

  • Lymphoplasmacytic Leukemia

  • Small Lymphocytic Lymphoma

  • Leukemia, Chronic Lymphatic

  • B-Cell Chronic Lymphocytic Leukaemia

  • Chronic Lymphatic Leukaemia

  • Lymphoplasmacytic Leukaemia

  • B Cell Chronic Lymphocytic Leukemia

  • Chronic B-Cell Lymphocytic Leukemia

  • Leukemia, Lymphocytic, Chronic

  • B-Cll

  • Chronic Lymphoid Leukemia

  • Leukemia Lymphocytic Chronic

  • Lymphoma Small Lymphocytic

  • Leukemia, Lymphocytic, Chronic, B-Cell

Lymphoma, Mucosa-Associated Lymphoid Type
  • Malt Lymphoma

  • Gastric Lymphoma, Primary

  • Lymphoma, Malt, Somatic

  • Mucosa-Associated Lymphoid Tissue Lymphoma

  • Extranodal Marginal Zone B-Cell Lymphoma

  • MALTOMA

  • Marginal Zone B-Cell Lymphoma

  • Mucosa-Associated Lymphatic Tissue Lymphoma

  • Primary Gastric Lymphoma

  • Gastric Lymphoma

  • Familial Primary Gastric Lymphoma

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris TNFRSF13C VGNC VGNC:54377
Felis catus TNFRSF13C VGNC VGNC:66405
Bos taurus TNFRSF13C VGNC VGNC:57365
Macaca mulatta TNFRSF13C VGNC VGNC:108067
Mus musculus TNFRSF13C MGD MGI:1919299
Rattus norvegicus TNFRSF13C RGD RGD:1560810
Others TNFRSF13C NCBI