Gene
CBLB
Cbl proto-oncogene B
- HGNC 1542↗(opens in a new tab)
- Ensembl gene ENSG00000114423↗(opens in a new tab)
- NCBI Gene 868↗(opens in a new tab)
Summary
- Cytogenetic location
- 3q13.11
- Coordinates
- Chromosome 3: 105,655,461–105,869,012 (GRCh38)
- Exons
- 19 exons across 213.6 kb
- Protein
- 982 amino acids
- Also known as
- RNF56, Cbl-b
- MANE Select transcript
- ENST00000394030.8NM_170662.5
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
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Autoimmune Disease
A disorder resulting from loss of function or tissue destruction of an organ or multiple organs, arising from humoral or cellular immune responses of the individual to their own tissue constituents. It may be systemic (e.g., systemic lupus erythematosus), or organ specific, (e.g., thyroiditis).
- 1 GenCC submitter rates it definitive or strong
How CBLB is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 6.7 kb of the gene's 213.6 kb; 2,949 of those bases code for the protein.
How a genome test reads CBLB
1
position in CBLB where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 213.6 kb of CBLB, introns included, not only the 6.7 kb of exons.
Genes linked to the same conditions
- AIREautoimmune regulatorShares 1 condition
- ATP2C1ATPase secretory pathway Ca2+ transporting 1Shares 1 condition
- C1QAcomplement C1q A chainShares 1 condition
- CASP10caspase 10Shares 1 condition
- CASP8caspase 8Shares 1 condition
- CHRNGcholinergic receptor nicotinic gamma subunitShares 1 condition
- CTLA4cytotoxic T-lymphocyte associated protein 4Shares 1 condition
- DNASE1L3deoxyribonuclease 1L3Shares 1 condition
- FASFas cell surface death receptorShares 1 condition
- FASLGFas ligandShares 1 condition
- FOXP3forkhead box P3Shares 1 condition
- KRASKRas proto-oncogene, GTPaseShares 1 condition
Traits linked to CBLB
The Human Phenotype Ontology lists these as features of the rare conditions CBLB can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). CBLB gene: Cbl proto-oncogene B. Retrieved 17 October 2026, from https://dantelabs.com/genes/cblb
Dante Labs. CBLB gene: Cbl proto-oncogene B [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/cblb
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