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Mutations in this gene may be associated with dentinogenesis imperfect and autosomal dominant amylogenesis imperfect

ITIH1 encodes a member of the inter-alpha-trypsin inhibitor family of proteins

SERPINA11 (Serpin Family A Member 11) is a Protein Coding gene

TMC8 Polyclonal Antibody, 20ul Diagnostic Probes & Oligos Cut through any challenge withEpidermodysplasia verruciformis (EV) is an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun exposed skin. EV is caused by mutations in either of two adjacent genes located on chromosome 17q25. Both of these genes encode integral membrane proteins that localize to the endoplasmic reticulum and are predicted to form transmembrane