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PMID 7661932
Gene Name YRRM1
Condition Azoospermia
Association The YRRM1 gene was involved in only three of them. The remaining seven patients showed deletion between DYS7C and DYS239 in common, indicating the presence of at least one additional gene, deletion of which causes azoospermia.
Population size 63
Population details 63 men with either azoospermia or severe oligospermia
Sex Male
Infertility type Male infertility
Other associated phenotypes Azoospermia


PCR analysis of the Y chromosome long arm in azoospermic patients: evidence for a second locus required for spermatogenesis

Kobayashi K, Mizuno K, Hida A, Komaki R, Tomita K, Matsushita I, Namiki M, Iwamoto T, Tamura S, Minowada S, et al.

We analyzed DNA from 63 Japanese men with either azoospermia or severe oligospermia whose Y chromosomes were cytogenetically normal. A total of 16 loci were examined: 15 loci on the long arm between DYS7E and DYZ1, and the YRRM1 locus, a candidate gene for the azoospermic factor, AZF. One patient with a pericentric inversion of the Y chromosome was also included. We detected micro-deletions in ten individuals. The YRRM1 gene was involved in only three of them. The remaining seven patients showed deletion between DYS7C and DYS239 in common, indicating the presence of at least one additional gene, deletion of which causes azoospermia. FAU - Kobayashi, K AU - Kobayashi K AD - Department of Human Genetics, School of International Health, University of Tokyo, Japan. FAU - Mizuno, K AU - Mizuno K FAU - Hida, A AU - Hida A FAU - Komaki, R AU - Komaki R FAU - Tomita, K AU - Tomita K FAU - Matsushita, I AU - Matsushita I FAU - Namiki, M AU - Namiki M FAU - Iwamoto, T AU - Iwamoto T FAU - Tamura, S AU - Tamura S