Gene
ADAM17
ADAM metallopeptidase domain 17
- HGNC 195↗(opens in a new tab)
- Ensembl gene ENSG00000151694↗(opens in a new tab)
- NCBI Gene 6868↗(opens in a new tab)
Summary
- Cytogenetic location
- 2p25.1
- Coordinates
- Chromosome 2: 9,488,486–9,555,830 (GRCh38)
- Exons
- 19 exons across 67.3 kb
- Protein
- 824 amino acids
- Also known as
- cSVP, CD156B
- Previous symbols
- TACE
- MANE Select transcript
- ENST00000310823.8NM_003183.6
- 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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Inflammatory Bowel Diseases (IBD)
- Inflammatory Bowel Disease
A spectrum of small and large bowel inflammatory diseases of unknown etiology. It includes Crohn's disease, ulcerative colitis, and colitis of indeterminate type.
- ClinGen rates the link definitive
- 4 GenCC submitters rate it definitive or strong
How ADAM17 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- 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 4.4 kb of the gene's 67.3 kb; 2,475 of those bases code for the protein.
How a genome test reads ADAM17
22
positions in ADAM17 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 67.3 kb of ADAM17, introns included, not only the 4.4 kb of exons.
Genes linked to the same conditions
Traits linked to ADAM17
The Human Phenotype Ontology lists these as features of the rare conditions ADAM17 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the integument
- Paronychia
- Thick nail
- Chronic monilial nail infection
- Generalized abnormality of skin
- Scaling skin
- Afro-textured hair
- Brittle hair
- Patchy baldness
Show 2 more traits
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.). ADAM17 gene: ADAM metallopeptidase domain 17. Retrieved 17 October 2026, from https://dantelabs.com/genes/adam17
Dante Labs. ADAM17 gene: ADAM metallopeptidase domain 17 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/adam17
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