Gene
IWS1
interacts with SUPT6H, CTD assembly factor 1
- HGNC 25467↗(opens in a new tab)
- Ensembl gene ENSG00000163166↗(opens in a new tab)
- NCBI Gene 55677↗(opens in a new tab)
Summary
- Cytogenetic location
- 2q14.3
- Coordinates
- Chromosome 2: 127,480,812–127,526,489 (GRCh38)
- Exons
- 14 exons across 45.7 kb
- Protein
- 819 amino acids
- Also known as
- DKFZp761G0123, FLJ10006, FLJ14655, FLJ32319
- MANE Select transcript
- ENST00000295321.9NM_017969.3
- 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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How IWS1 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 3 kb of the gene's 45.7 kb; 2,460 of those bases code for the protein.
External links
Gene records
Transcript
Protein
Clinical
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.
Cite this page
Dante Labs. (n.d.). IWS1 gene: interacts with SUPT6H, CTD assembly factor 1. Retrieved 16 October 2026, from https://dantelabs.com/genes/iws1
Dante Labs. IWS1 gene: interacts with SUPT6H, CTD assembly factor 1 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/iws1
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