69487-7LOINC 2.82
TNFRSF13B gene full mutation analysis in Blood or Tissue by Sequencing
TNFRSF13B gene Full Mut Anl Bld/T Seq
Definition
- Sequencing of the entire coding region (full gene sequencing) within the TNFRSF13B gene (also known as TACI gene) is performed to identify mutations or variants in individuals with clinical features such as common variable immunodeficiency (CVID), selective IgA deficiency, lymphoproliferative disease associated with CVID, and autoimmune phenotypes with CVID. The TNFRSF13B gene, located on chromosome 17, consists of 5 exons spanning approximately 35 kb.
Component
- TNFRSF13B gene full mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Find
Scale
- Doc
Method
- Sequencing
Related names
- BAFF; Blood; BLYS; CD267; CVID; CVID2; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; IGAD2; Inherited; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutations; Next generation sequencing; NGS; Point in time; Random; RYZN; sequencing of entire coding region; TACI; TALL1; THANK; Tissue; Tissue, unspecified; TNFRSF14B; TNFSF20; Tumor necrosis factor (ligand) superfamily, member 13b; tumor necrosis factor receptor superfamily, member 13B; WB; Whole blood; Whole blood or Tissue; ZTNF4
Index terms
- BAFF
- Blood
- BLYS
- CD267
- CVID
- CVID2
- Document
- Finding
- Findings
- full gene sequencing
- Full Mut Anl
- Genetics
- Heredity
- Heritable
- high-throughput sequencing
- HTS
- IGAD2
- Inherited
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mutations
- Next generation sequencing
- NGS
- Point in time
- Random
- RYZN
- sequencing of entire coding region
- TACI
- TALL1
- THANK
- Tissue
- Tissue, unspecified
- TNFRSF14B
- TNFSF20
- Tumor necrosis factor (ligand) superfamily, member 13b
- tumor necrosis factor receptor superfamily, member 13B
- WB
- Whole blood
2 further terms