Gene
SOST
sclerostin
- HGNC 13771↗(opens in a new tab)
- Ensembl gene ENSG00000167941↗(opens in a new tab)
- NCBI Gene 50964↗(opens in a new tab)
Summary
- Cytogenetic location
- 17q21.31
- Coordinates
- Chromosome 17: 43,753,738–43,758,791 (GRCh38)
- Exons
- 2 exons across 5.1 kb
- Protein
- 213 amino acids
- Inheritance
- Autosomal recessive
- Also known as
- VBCH, DAND6
- MANE Select transcript
- ENST00000301691.3NM_025237.3
- 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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Sclerosing Bone Dysplasias (High Bone Mass)
- SclerosteosisAutosomal recessive
A progressive bone overgrowth condition caused by SOST or LRP4 variants, with skull thickening, cranial nerve compression and often fused fingers.
- 3 GenCC submitters rate it definitive or strong
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 SOST is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
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 2.3 kb of the gene's 5.1 kb; 642 of those bases code for the protein.
How a genome test reads SOST
5
positions in SOST 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 5.1 kb of SOST, introns included, not only the 2.3 kb of exons.
Traits linked to SOST
The Human Phenotype Ontology lists these as features of the rare conditions SOST can cause. Each trait's page lists the other genes linked to it.
Abnormality of head or neck
- Abnormal dental position
- Big lower jaw
- Big sella turcica
- Boxer's nasal deformity
- Craniofacial osteosclerosis
- Depressed nasal bridge
- Enlargement of craniofacial bones
- Frontal bossing
Show 14 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.). SOST gene: sclerostin. Retrieved 17 October 2026, from https://dantelabs.com/genes/sost
Dante Labs. SOST gene: sclerostin [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/sost
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