Gene
CTSB
cathepsin B
- HGNC 2527↗(opens in a new tab)
- Ensembl gene ENSG00000164733↗(opens in a new tab)
- NCBI Gene 1508↗(opens in a new tab)
Summary
- Cytogenetic location
- 8p23.1
- Coordinates
- Chromosome 8: 11,842,524–11,868,087 (GRCh38)
- Exons
- 10 exons across 25.6 kb
- Protein
- 339 amino acids
- MANE Select transcript
- ENST00000353047.11NM_001908.5
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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How CTSB 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 3.7 kb of the gene's 25.6 kb; 1,020 of those bases code for the protein.
Traits linked to CTSB
The Human Phenotype Ontology lists these as features of the rare conditions CTSB 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.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
Cite this page
Dante Labs. (n.d.). CTSB gene: cathepsin B. Retrieved 16 October 2026, from https://dantelabs.com/genes/ctsb
Dante Labs. CTSB gene: cathepsin B [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/ctsb
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