TY  - JOUR
A1  - MacMurray, Armand J.
A1  - Moralejo, Daniel H.
A1  - Kwitek, Anne E.
A1  - Rutledge, Elizabeth A.
A1  - Van Yserloo, Brian
A1  - Gohlke, Paul
A1  - Speros, Sara J.
A1  - Snyder, Ben
A1  - Schaefer, Jonathan
A1  - Bieg, Sabine
A1  - Jiang, Jianjie
A1  - Ettinger, Ruth A.
A1  - Fuller, Jessica
A1  - Daniels, Terri L.
A1  - Pettersson, Anna
A1  - Orlebeke, Kimberly
A1  - Birren, Bruce
A1  - Jacob, Howard J.
A1  - Lander, Eric S.
A1  - Lernmark, Åke
T1  - Lymphopenia in the BB Rat Model of Type 1 Diabetes is Due to a Mutation in a Novel Immune-Associated Nucleotide (Ian)-Related Gene
Y1  - 2002/07/01 
JF  - Genome Research 
JO  - Genome Research 
SP  - 1029 
EP  - 1039 
DO  - 10.1101/gr.412702 
VL  - 12 
IS  - 7 
UR  - http://genome.cshlp.org/content/12/7/1029.abstract 
N2  - The BB (BioBreeding) rat is one of the best models of spontaneous autoimmune diabetes and is used to study non-MHC loci contributing to Type 1 diabetes. Type 1 diabetes in the diabetes-prone BB (BBDP) rat is polygenic, dependent upon mutations at several loci.Iddm1, on chromosome 4, is responsible for a lymphopenia (lyp) phenotype and is essential to diabetes. In this study, we report the positional cloning of theIddm1/lyp locus. We show that lymphopenia is due to a frameshift deletion in a novel member (Ian5) of the Immune-Associated Nucleotide (IAN)-related gene family, resulting in truncation of a significant portion of the protein. This mutation was absent in 37 other inbred rat strains that are nonlymphopenic and nondiabetic. The IAN gene family, lying within a tight cluster on rat chromosome 4, mouse chromosome 6, and human chromosome 7, is poorly characterized. Some members of the family have been shown to be expressed in mature T cells and switched on during thymic T-cell development, suggesting thatIan5 may be a key factor in T-cell development. The lymphopenia mutation may thus be useful not only to elucidate Type 1 diabetes, but also in the function of the Ian gene family as a whole.[Sequence data reported in this paper has been deposited in GenBank and assigned the following accession nos:AF517674, AF517675, AF517676, and AF517677. Supplemental material is available online at http://depts.washington.edu/rhwlab/ and http:www.genome.org. ] The following individuals and institutions kindly provided reagents, samples, or unpublished information as indicated in the paper: K. Matsumoto and the Sir Frederick Banting Research Centre. 
ER  -