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Protein-coding gene in humans
protein 8 is an enzyme that in humans is encoded by the CHD8 gene. The gene CHD8 encodes the protein chromodomain helicase DNA binding protein 8
CHD8
Family of regulator genes
c-Myc. Myc has been shown to interact with: ACTL6A BRCA1 Bcl-2 Cyclin T1 CHD8 DNMT3A EP400 GTF2I HTATIP let-7 MAPK1 MAPK8 MAX MLH1 MYCBP2 MYCBP NMI NFYB
Myc
Genetic mutation not inherited from a parent
large scale WES study of autism families found that de novo mutations in CHD8 were strongly associated with autism spectrum disorder, leading to dysregulated
De_novo_mutation
Protein-coding gene in humans
genes are mutated in three or more people with autism. These six genes — CHD8, DYRK1A, ANK2, GRIN2B, DSCAM and CHD2 — are the strongest autism candidates
CHD2
Class of enzymes that unpack genetic material
helicase DNA binding protein: CHD1, CHD1L, CHD2, CHD3, CHD4, CHD5, CHD6, CHD7, CHD8, CHD9 DEAD box/DEAD/DEAH box helicase: DDX3X, DDX5, DDX6, DDX10, DDX11, DDX12
Helicase
Protein-coding gene
2007.07.011. PMID 17707600. Yuan CC, Zhao X, Florens L, et al. (2007). "CHD8 associates with human Staf and contributes to efficient U6 RNA polymerase
ZNF143
Israeli computational biologist
Witherspoon, Kali; Gerdts, Jennifer; Baker, Carl (2014-07-17). "Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development". Cell. 158 (2):
Osnat_Penn
Family of proteins that play a role in chromatin remodeling
A, Young AN, Ruiz NB, Buness A, Sant GM, Arnold M, et al. (April 2021). "Chd8 regulates X chromosome inactivation in mouse through fine-tuning control
Polycomb-group_proteins
HGNC:16816; Q8TDI0 2932 CHD6 HGNC:19057; Q8TD26 2933 CHD7 HGNC:20626; Q9P2D1 2934 CHD8 HGNC:20153; Q9HCK8 2935 CHD9 HGNC:25701; Q3L8U1 2936 CHD9NB HGNC:53436; A0A1B0GV96
List of human protein-coding genes 2
List_of_human_protein-coding_genes_2
(00:56)". USGS. Retrieved 22 July 2014. "Genetic link to autism found, known as CHD8 mutation". Science Daily. 3 July 2014. Retrieved 6 July 2014. Robertson,
2014_in_science
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