TCF20 Polyclonal Antibody, 50ul Cell Culture Mutations in this gene are

Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI)

This endoplasmic reticulum membrane protein catalyzes the first reaction in the cholesterol catabolic pathway in the liver

Transcripts may include the shared exon spliced to the gene-specific exons

This gene encodes a member of the zinc fingers and homeoboxes (ZHX) gene family

Contains 2 PAH (paired amphipathic helix) repeats

TCF20 Polyclonal Antibody, 50ul Cell Culture Mutations in this gene areThis gene encodes a transcription factor that recognizes the platelet derived growth factor responsive element in the matrix metalloproteinase 3 promoter. The encoded protein is thought to be a transcriptional coactivator, enhancing the activity of transcription factors such as JUN and SP1. Mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants.