CHD7 wt Allele

Human CHD7 wild-type allele is located in the vicinity of 8q12.2 and is approximately 188 kb in length. This allele, which encodes chromodomain-helicase-DNA-binding protein 7, may be involved in both transcriptional regulation and chromatin modification. Mutation of the gene is associated with CHARGE syndrome. (NCI Thesaurus)

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CHD7 Gene

This gene may play a role in the modulation of both chromatin structure modification and transcription.

CHD5 wt Allele

Human CHD5 wild-type allele is located in the vicinity of 1p36.3 and is approximately 78 kb in length. This allele, which encodes…

CHD5 Gene

This gene is involved in both chromatin structure regulation and tumor suppression.

CHD2 wt Allele

Human CHD2 wild-type allele is located in the vicinity of 15q26 and is approximately 125 kb in length. This allele, which encodes…

CHD2 Gene

This gene may be involved in the regulation of both gene expression and chromatin modification.

CHD1 wt Allele

Human CHD1 wild-type allele is located within 5q15-q21 and is approximately 71 kb in length. This allele, which encodes chromodomain-helicase-DNA-binding protein 1,…