Gene
SOX11
SRY-box transcription factor 11
- HGNC 11191↗(opens in a new tab)
- Ensembl gene ENSG00000176887↗(opens in a new tab)
- NCBI Gene 6664↗(opens in a new tab)
Summary
- Cytogenetic location
- 2p25.2
- Coordinates
- Chromosome 2: 5,692,384–5,701,385 (GRCh38)
- Exons
- 1 exon across 9 kb
- Protein
- 441 amino acids
- MANE Select transcript
- ENST00000322002.5NM_003108.4
- 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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No Genome Test report reads SOX11 yet. The test sequences your whole genome, so your data includes it all the same.
How SOX11 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 9 kb of the gene's 9 kb; 1,326 of those bases code for the protein.
How a genome test reads SOX11
48
positions in SOX11 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 9 kb of SOX11, introns included, not only the 9 kb of exons.
Traits linked to SOX11
The Human Phenotype Ontology lists these as features of the rare conditions SOX11 can cause. Each trait's page lists the other genes linked to it.
Abnormality of head or neck
- Abnormally small head
- Drooping lower lip
- Full cheeks
- Coarse facial features
- Full lower lip
- Prominent eyelashes
- Thick eyebrow
- Wide mouth
Show 27 more traits
- Abnormal facial shape
- Broad nasal tip
- Broad philtrum
- Delayed eruption of teeth
- Depressed nasal bridge
- Flattened bony protrusion above eyes
- Full lips
- High palate
- Highly arched eyebrow
- Long eyelashes
- Long nose
- Low frontal hairline
- Low hanging columella
- Midface retrusion
- Nasal tip, upturned
- Open mouth
- Recurrent colds
- Short chin
- Short nose
- Short opening between the eyelids
- Short philtrum
- Sparse scalp hair
- Thick nasal alae
- Thin red part of the upper lip
- Underdeveloped tissue around nostril
- Wide nasal base
- Dandy-Walker malformation
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.
- 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.). SOX11 gene: SRY-box transcription factor 11. Retrieved 17 October 2026, from https://dantelabs.com/genes/sox11
Dante Labs. SOX11 gene: SRY-box transcription factor 11 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/sox11
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