IGLJ3
Chr 22immunoglobulin lambda joining 3
Also known as: J3
45
ClinVar variants
25
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— IGLJ3
📋
ClinVar Variants
25 Pathogenic / Likely Pathogenic· 18 VUS of 45 total submissions
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
45 submitted variants in ClinVar
Classification Summary
Pathogenic23
Likely Pathogenic2
VUS18
Likely Benign1
Conflicting1
23
Pathogenic
2
Likely Pathogenic
18
VUS
1
Likely Benign
1
Conflicting
Curated Variants Distribution
Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable
| Classification | LoF | Missense + Inframe | Non-coding | Synonymous | Total |
|---|---|---|---|---|---|
Pathogenic | — | — | — | — | 23 |
Likely Pathogenic | — | — | — | — | 2 |
VUS | — | — | — | — | 18 |
Likely Benign | — | — | — | — | 1 |
Benign | — | — | — | — | 0 |
Conflicting | — | 1 | |||
| Total | — | 45 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
IGLJ3 · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
OMIM — Genotype-Phenotype
No OMIM entries found.
External Resources
Links to major genomics databases and tools
Variant Interpretation
Population Databases
Gene Resources
Expert Curation
ClinGen
Expert-curated gene-disease validity
GenCC
Gene Curation Coalition — multi-curator classifications
Orphanet
Rare disease encyclopedia and gene-disease associations
SFARI Gene
Autism-gene association scoring (SFARI)
PanelApp
Gene panels for rare disease diagnostics (Genomics England)
LOVD
Leiden Open Variation Database — variant listings
GeneReviews
Expert-authored summaries of heritable conditions (NCBI)
Clinical Literature
Landmark / reviewRecent case evidence
Key Publications
Landmark & review papers · by relevance
Immunoglobulin variable domain high-throughput sequencing reveals specific novel mutational patterns in POEMS syndrome.
Bender S et al.·Blood
2020
[Differentially expressed genes between upward and downward progressing types of nasopharyngeal carcinoma].
Liang WJ et al.·Ai Zheng
2008
Lack of allelic exclusion by secondary rearrangements of tumour B-cell receptor light chains in hairy cell leukaemia.
Sozzi E et al.·Hematol Oncol
2011
Top 10 resultsSearch PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
No open access results found
Top 5 resultsSearch Europe PMC ↗
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →External Resources
Links to major genomics databases and tools
Variant Interpretation
Population Databases
Gene Resources
Expert Curation
ClinGen
Expert-curated gene-disease validity
GenCC
Gene Curation Coalition — multi-curator classifications
Orphanet
Rare disease encyclopedia and gene-disease associations
SFARI Gene
Autism-gene association scoring (SFARI)
PanelApp
Gene panels for rare disease diagnostics (Genomics England)
LOVD
Leiden Open Variation Database — variant listings
GeneReviews
Expert-authored summaries of heritable conditions (NCBI)