CHD8
Chromodomain helicase DNA-binding protein 8
AF-Q9HCK8-F1 · v6 · Human reference sequence 1–2,581
Predicted backbone
≥9070–<9050–<70<50
Research links
Autism spectrum disorder
Rare variant study
A sequencing study reports recurrent disruptive CHD8 variants and characterizes the individuals carrying them.
Provenance and confidence
AlphaFold DB prediction by Google DeepMind and EMBL-EBI. The viewer draws a Cα trace derived from the RCSB BinaryCIF copy. We matched the release, residue sequence and mean pLDDT against AlphaFold DB.
- Model
- AF-Q9HCK8-F1 · v6
- Retrieved
- Mean pLDDT
- 53.92 / 100
- Residues by band
- ≥90 · 143 / 70–<90 · 861 / 50–<70 · 240 / <50 · 1,337
- Coordinate SHA-256
aeeadee5becd2572d1fe4700c09e6cede1c1e83f7af467246d5e7d2b7f671629- License
- CC BY 4.0