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 chromodomain-helicase-DNA-binding protein 2, may play a role in the modulation of both chromatin structure and gene expression. Deletion of this gene may be associated with congenital diaphragmatic hernia. (NCI Thesaurus)

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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,…

CHD1 Gene

This gene is involved in the modification of chromatin structure.

CHCHD7/PLAG1 Fusion Gene

A fusion gene that results from a chromosomal inversion inv(8)(q12.1;q12.1) which fuses non-coding exon 1 of the CHCHD7 gene upstream of the…

CHCHD7 wt Allele

Human CHCHD7 wild-type allele is located in the vicinity of 8q12.1 and is approximately 7 kb in length. This allele, which encodes…

CHCHD7 Gene

This gene may be involved in stature.