HMGN1 wt Allele

Human HMGN1 wild-type allele is located in the vicinity of 21q22.2 and is approximately 7 kb in length. This allele, which encodes nonhistone chromosomal protein HMG-14 protein, is involved in the modulation of chromatin modifications. The HMGN1 gene is overexpressed in Down syndrome. (NCI Thesaurus)

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HMGN1 Gene

This gene is involved in chromatin remodeling and enhancing gene transcription from chromatin templates.

HMGN Family Protein

The high mobility group N (HMGN) proteins are a family of nuclear proteins that binds to nucleosomes, changes the architecture of chromatin,…

HMGN Family Gene

Human HMGN Family Genes encode nuclear HMGN proteins that bind to nucleosomes, change chromatin architecture, and enhance transcription or replication. They typically…

HMGCR wt Allele

Human HMGCR wild-type allele is located within 5q13.3-q14 and is approximately 25 kb in length. This allele, which encodes 3-hydroxy-3-methylglutaryl-coenzyme A reductase…

HMGCR Gene

This gene plays a role in the biosynthesis of steroids.

HMGB3 wt Allele

Human HMGB3 wild-type allele is located within Xq28 and is approximately 6 kb in length. This allele, which encodes high mobility group…