Gene
ADAMTS9
ADAM metallopeptidase with thrombospondin type 1 motif 9
- HGNC 13202↗(opens in a new tab)
- Ensembl gene ENSG00000163638↗(opens in a new tab)
- NCBI Gene 56999↗(opens in a new tab)
Summary
- Cytogenetic location
- 3p14.1
- Coordinates
- Chromosome 3: 64,515,654–64,688,000 (GRCh38)
- Exons
- 40 exons across 172.3 kb
- Protein
- 1,935 amino acids
- Inheritance
- Autosomal recessive
- Also known as
- KIAA1312
- MANE Select transcript
- ENST00000498707.5NM_182920.2
- 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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Get my Genome TestCurated report relevant to this gene
Nephronophthisis and Senior-Løken Syndrome
- NephronophthisisAutosomal recessive
A recessively inherited kidney disease, caused by variants in NPHP1 and other cilia genes, in which progressive tubulointerstitial scarring leads to kidney failure, typically in the first three decades of life.
- 1 GenCC submitter rates it definitive or strong
What knowing changes
Knowing allows regular kidney function monitoring, timely planning for dialysis or transplantation, and carrier testing for relatives.
Inheritance
- Autosomal recessive
- It takes a changed copy from each parent. With one, you are a carrier and usually unaffected; when both parents are carriers, each child has a one-in-four chance of inheriting two.
How ADAMTS9 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 7.6 kb of the gene's 172.3 kb; 5,808 of those bases code for the protein.
Genes linked to the same conditions
- ANKS6ankyrin repeat and sterile alpha motif domain containing 6Shares 1 condition
- CEP164centrosomal protein 164Shares 1 condition
- CEP83centrosomal protein 83Shares 1 condition
- DCDC2doublecortin domain containing 2Shares 1 condition
- GLIS2GLIS family zinc finger 2Shares 1 condition
- INVSinversinShares 1 condition
- MAPKBP1mitogen-activated protein kinase binding protein 1Shares 1 condition
- NEK8NIMA related kinase 8Shares 1 condition
- NPHP1nephrocystin 1Shares 1 condition
- NPHP3nephrocystin 3Shares 1 condition
- NPHP4nephrocystin 4Shares 1 condition
- TMEM67transmembrane protein 67Shares 1 condition
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.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). ADAMTS9 gene: ADAM metallopeptidase with thrombospondin type 1 motif 9. Retrieved 16 October 2026, from https://dantelabs.com/genes/adamts9
Dante Labs. ADAMTS9 gene: ADAM metallopeptidase with thrombospondin type 1 motif 9 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/adamts9
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