About Us

Search Results



PMID 11095425
Gene Name INSL3
Condition Infertility
Association The study concludes that frequency of INSL3/RLF gene mutations as a cause of cryptorchidism is low, because only 2 of 145 (1.4%) formerly cryptorchid patients were found to have mutations

PMID 11095425
Gene Name INSL3
Condition Cryptorchidism
Association Two mutations, R49X and P69L, and several polymorphisms were identified. Both mutations were located in the connecting peptide region of the protein. The frequency of INSL3/RLF gene mutations as a cause of cryptorchidism is low, because only 2 of 145 (1.4
PMID 11095425
Gene Name INSL3
Condition Cryptorchidism
Association Two mutations, R49X and P69L, and several polymorphisms were identified. Both mutations were located in the connecting peptide region of the protein. The frequency of INSL3/RLF gene mutations as a cause of cryptorchidism is low, because only 2 of 145 (1.4
Mutation R49X and P69L
Population size 181
Population details 181 145 formerly cryptorchid patients, 36 adult male controls()
Sex Male
Infertility type Male infertility
Associated genes INSL3/RLF
Other associated phenotypes Cryptorchidism


Insulin-like 3/relaxin-like factor gene mutations are associated with cryptorchidism

Tomboc M, Lee PA, Mitwally MF, Schneck FX, Bellinger M, Witchel SF.

Cryptorchidism is a common anomaly of male sexual differentiation. Two phases of testicular descent are recognized, transabdominal and inguinoscrotal. With evidence that androgens and Müllerian inhibitory hormone were not completely responsible for testicular descent, the existence of a third testicular hormone mediating testicular descent was postulated. Insulin-like 3 (INSL3) [also known as relaxin-like factor (RLF) and Leydig insulin-like protein (LEY I-L)] is a member of the insulin/relaxin hormone superfamily that is highly expressed in Leydig cells. The phenotype of transgenic mice with targeted deletion of the Insl3 gene was bilateral cryptorchidism with morphological evidence of abnormal gubernacular development. With this implicit evidence that Insl3 mediates testicular descent in mice, we performed mutation detection analysis of the coding regions of the 2 exon INSL3 gene in genomic DNA samples obtained from 145 formerly cryptorchid patients and 36 adult male controls. Single-strand conformational polymorphism analysis was used for the mutation detection studies. Two mutations, R49X and P69L, and several polymorphisms were identified. Both mutations were located in the connecting peptide region of the protein. The frequency of INSL3/RLF gene mutations as a cause of cryptorchidism is low, because only 2 of 145 (1.4%) formerly cryptorchid patients were found to have mutations. FAU - Tomboc, M AU - Tomboc M AD - Division of Pediatric Endocrinology, Children's Hospital of Pittsburgh, University of Pittsburgh, Pennsylvania 15213, USA. FAU - Lee, P A AU - Lee PA FAU - Mitwally, M F AU - Mitwally MF FAU - Schneck, F X AU - Schneck FX FAU - Bellinger, M AU - Bellinger M