Gene
YY1
YY1 transcription factor
- HGNC 12856↗(opens in a new tab)
- Ensembl gene ENSG00000100811↗(opens in a new tab)
- NCBI Gene 7528↗(opens in a new tab)
Summary
- Cytogenetic location
- 14q32.2
- Coordinates
- Chromosome 14: 100,239,144–100,282,788 (GRCh38)
- Exons
- 5 exons across 43.6 kb
- Protein
- 414 amino acids
- Also known as
- NF-E1, DELTA, UCRBP, YIN-YANG-1, INO80S
- MANE Select transcript
- ENST00000262238.10NM_003403.5
- 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.
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No Genome Test report reads YY1 yet. The test sequences your whole genome, so your data includes it all the same.
How YY1 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 6.5 kb of the gene's 43.6 kb; 1,245 of those bases code for the protein.
How a genome test reads YY1
18
positions in YY1 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 43.6 kb of YY1, introns included, not only the 6.5 kb of exons.
Traits linked to YY1
The Human Phenotype Ontology lists these as features of the rare conditions YY1 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Delayed speech and language development
- Intellectual disability
- Motor delay
- Epilepsy
- Global developmental delay
- Transient global amnesia
- Tremor
- Behavioral abnormality
Show 34 more traits
- Delayed ability to walk
- Disturbances of consciousness
- Fluctuations in consciousness
- Increased appetite
- Intellectual disability, mild
- IQ between 34 and 49
- Abnormal cerebral white matter morphology
- Abnormal rapid eye movement sleep
- Abnormality of mental function
- Abnormality of pain sensation
- Absent speech development
- Agenesis of corpus callosum
- Anxiety
- Attention deficit
- Autism
- Autism spectrum disorder
- Cancer of early nerve cells
- Coma
- Cortical dysplasia
- Delayed CNS myelination
- Delayed myelination
- Difficulty sleeping
- Difficulty staying or falling asleep
- Dystonia
- Gliosis
- Intellectual disability, severe
- Lateral ventricle dilatation
- Lethargy
- Pins and needles feeling
- Severe global developmental delay
- Toe walking
- Underdevelopment of part of brain called corpus callosum
- Ventriculomegaly
- Waddling gait
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.). YY1 gene: YY1 transcription factor. Retrieved 16 October 2026, from https://dantelabs.com/genes/yy1
Dante Labs. YY1 gene: YY1 transcription factor [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/yy1
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