Identity
HGNC
LOCATION
17p11.2
LOCUSID
ALIAS
CD267,CVID,CVID2,IGAD2,RYZN,TACI,TNFRSF14B
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 23495
MIM: 604907
HGNC: 18153
Ensembl: ENSG00000240505
Variants:
dbSNP: 23495
ClinVar: 23495
TCGA: ENSG00000240505
COSMIC: TNFRSF13B
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36305039 | 2023 | TNFRSF13B/TACI Mutations in Patients with Chronic Rhinosinusitis with Nasal Polyps. | 0 |
| 37272840 | 2023 | Features of Isoforms of Human Soluble TACI. | 0 |
| 37534633 | 2023 | TNFRSF13B gene mutation in familial acute myeloid leukemia: A new piece in the complex scenario of hereditary predisposition? | 0 |
| 36305039 | 2023 | TNFRSF13B/TACI Mutations in Patients with Chronic Rhinosinusitis with Nasal Polyps. | 0 |
| 37272840 | 2023 | Features of Isoforms of Human Soluble TACI. | 0 |
| 37534633 | 2023 | TNFRSF13B gene mutation in familial acute myeloid leukemia: A new piece in the complex scenario of hereditary predisposition? | 0 |
| 34922003 | 2022 | Resolving the polygenic aetiology of a late onset combined immune deficiency caused by NFKB1 haploinsufficiency and modified by PIK3R1 and TNFRSF13B variants. | 2 |
| 35017485 | 2022 | A BAFF ligand-based CAR-T cell targeting three receptors and multiple B cell cancers. | 24 |
| 35686370 | 2022 | TACI variants as underlying condition in autoimmune neutropenia: Description of four cases. | 1 |
| 34922003 | 2022 | Resolving the polygenic aetiology of a late onset combined immune deficiency caused by NFKB1 haploinsufficiency and modified by PIK3R1 and TNFRSF13B variants. | 2 |
| 35017485 | 2022 | A BAFF ligand-based CAR-T cell targeting three receptors and multiple B cell cancers. | 24 |
| 35686370 | 2022 | TACI variants as underlying condition in autoimmune neutropenia: Description of four cases. | 1 |
| 33586470 | 2021 | TNFRSF13B c.226G>A (p.Gly76Ser) as a Novel Causative Mutation for Pulmonary Arterial Hypertension. | 8 |
| 34247095 | 2021 | TACI deficiency - a complex system out of balance. | 13 |
| 34283811 | 2021 | TNFRSF13B genotypes control immune-mediated pathology by regulating the functions of innate B cells. | 3 |
Citation
Dessen P
TNFRSF13B (TNF receptor superfamily member 13B)
Atlas Genet Cytogenet Oncol Haematol. 2003-06-01
Online version: http://atlasgeneticsoncology.org/gene/42613/tnfrsf13b-(tnf-receptor-superfamily-member-13b)
