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Publication : Skeletal dysplasia and male infertility locus on mouse chromosome 9.

First Author  Cha KB Year  2004
Journal  Genomics Volume  83
Issue  6 Pages  951-60
PubMed ID  15177549 Mgi Jnum  J:90436
Mgi Id  MGI:3043863 Doi  10.1016/j.ygeno.2003.12.020
Citation  Cha KB, et al. (2004) Skeletal dysplasia and male infertility locus on mouse chromosome 9. Genomics 83(6):951-60
abstractText  In mice and humans, growth insufficiency and male infertility are common disorders that are genetically and phenotypically complex. We describe a spontaneously arising mouse mutant, chagun, that is affected by both dwarfism and male infertility. Dwarfism disproportionately affects long bones and is characterized by a defect in the proliferative zone of chondrocytes in the growth plate. Gonads of mutant males are small, with apparent germ cell loss and no evidence of mature sperm. The locus responsible for chagun is recessive and maps to distal chromosome 9, in a region homologous to human chromosome 3. This location is consistent with chagun defining a novel locus. Identification of the mutant gene will uncover the basis for another type of skeletal dysplasia and male infertility.
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