| Literature DB >> 31149201 |
T C Zhou1,2, Y Yang1,2, L Zhang1, Y Y Liu1, X Lai1, Y Li1, X Li1, Y X Xiong1, L Yang3, D M Irwin2,4.
Abstract
No inheritance of early-onset female-related type 2 diabetes was reported within Chinese families. In this study, we aim to describe the inheritance pattern of type 2 diabetes in a 3-generation family and identify the gene responsible for type 2 diabetes. Genome-wide multipoint parametric linkage analysis revealed a maximum multipoint logarithm of odds (lod) score of 2.1 for a locus being associated with type 2 diabetes in this family on chromosome 20p11.2-12 between 23.5~30.8cM. Type 2 diabetes may be transmitted as an autosomal dominant trait with a high female-related penetrance in this family. Here we describe the first genetic locus for type 2 diabetes at chromosome 20p11.2-12. This region contains 8 known or predicted genes (PLCB1, PLCB4, LAMP5, PAK7, ANKEF1, SNAP25, SLX4IP, and JAG1). Gene SNAP25 which linked to energy or glucose homeostasis associated phenotypes may play a role in the development of type 2 diabetes in this family.Entities:
Keywords: chromosome 20p11.2-12; linkage analysis; type 2 diabetes family
Year: 2017 PMID: 31149201 PMCID: PMC6516578 DOI: 10.4183/aeb.2017.364
Source DB: PubMed Journal: Acta Endocrinol (Buchar) ISSN: 1841-0987 Impact factor: 0.877