EHMT1 wt Allele

Human EHMT1 wild-type allele is located in the vicinity of 9q34.3 and is approximately 139 kb in length. This allele, which encodes histone-lysine N-methyltransferase, H3 lysine-9 specific 5 protein, plays a role in the modulation of histone methylation. Mutation of the gene is associated with chromosome 9q subtelomeric deletion syndrome. (NCI Thesaurus)

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EHMT1 Gene

This gene is involved in histone methylation.

Ehlers-Danlos Syndrome

An inherited connective tissue disorder characterized by loose and fragile skin and joint hypermobility.

EHF wt Allele

Human EHF wild-type allele is located in the vicinity of 11p12 and is approximately 40 kb in length. This allele, which encodes…

EHF Gene

This gene is involved in transcriptional repression.

Egyptian

Denotes the inhabitants of Egypt, a person from there, or their descendants elsewhere.

EGR1 wt Allele

Human EGR1 wild-type allele is located within 5q23-q31 and is approximately 4 kb in length. This allele, which encodes early growth response…