Gene
ITGB6
integrin subunit beta 6
- HGNC 6161↗(opens in a new tab)
- Ensembl gene ENSG00000115221↗(opens in a new tab)
- NCBI Gene 3694↗(opens in a new tab)
Summary
- Cytogenetic location
- 2q24.2
- Coordinates
- Chromosome 2: 160,099,671–160,200,272 (GRCh38)
- Exons
- 15 exons across 100.6 kb
- Protein
- 788 amino acids
- Inheritance
- Autosomal dominant
- MANE Select transcript
- ENST00000283249.7NM_000888.5
- 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.
Read ITGB6, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated report relevant to this gene
Amelogenesis Imperfecta
- Autosomal dominant
- 2 GenCC submitters rate it definitive or strong
Inheritance
- Autosomal dominant
- One changed copy, from either parent, is enough. A parent who has one passes it on to each child with a one-in-two chance.
How ITGB6 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 4.6 kb of the gene's 100.6 kb; 2,367 of those bases code for the protein.
How a genome test reads ITGB6
7
positions in ITGB6 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 100.6 kb of ITGB6, introns included, not only the 4.6 kb of exons.
Genes linked to the same conditions
- ACP4acid phosphatase 4Shares 1 condition
- AMBNameloblastinShares 1 condition
- AMELXamelogenin X-linkedShares 1 condition
- DLX3distal-less homeobox 3Shares 1 condition
- ENAMenamelinShares 1 condition
- FAM20AFAM20A golgi associated secretory pathway pseudokinaseShares 1 condition
- GPR68G protein-coupled receptor 68Shares 1 condition
- KLK4kallikrein related peptidase 4Shares 1 condition
- LAMB3laminin subunit beta 3Shares 1 condition
- MMP20matrix metallopeptidase 20Shares 1 condition
- ODAPHodontogenesis associated phosphoproteinShares 1 condition
- RELTRELT TNF receptorShares 1 condition
Traits linked to ITGB6
The Human Phenotype Ontology lists these as features of the rare conditions ITGB6 can cause. Each trait's page lists the other genes linked to it.
Abnormality of head or neck
- Abnormally small head
- Sparse or absent eyebrows
- Sparse scalp hair
- Absence of overlap of anterior upper and lower teeth
- Abnormal of nasal shape
- Amelogenesis imperfecta
- Dental enamel pits
- Thin dental enamel
Show 1 more trait
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.). ITGB6 gene: integrin subunit beta 6. Retrieved 17 October 2026, from https://dantelabs.com/genes/itgb6
Dante Labs. ITGB6 gene: integrin subunit beta 6 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/itgb6
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks