WDR11

WDR11

A gene on chromosome 10q26 that encodes a member of the WD-repeat protein family, which are involved in various cellular processes, including cell cycle progression, signal transduction, apoptosis and gene regulation. WDR11 is located in a chromosome region frequently deleted in gliomas and tumours of other tissues, suggesting that it may be a tumour suppressor.
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References in periodicals archive ?
The WDR11 gene product partners EMX1, a homeodomain transcription factor involved in the development of olfactory neurons.
WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
Digenic Inheritance of PROKR2 and WDR11 Mutations in Pituitary Stalk Interruption Syndrome.
Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism
WDR11. The WDR11 gene, on chromosome 10q26, encodes for a 1224 amino acid protein, originally identified as a potential tumor suppressor in human glioblastoma cells [90].
Layman, "The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome," Molecular and Cellular Endocrinology, vol.
Malaj et al., "A novel member of the WD-repeat gene family, WDR11, maps to the 10q26 region and is disrupted by a chromosome translocation in human glioblastoma cells," Oncogene, vol.
Central hypogonadotropic hypogonadism: genetic complexity of a complex disease
To date, at least 17 genes have been associated with KS and these include KAL1, FGFR1, PROK2, PROKR2, FGF8, HS6ST1, CHD7, WDR11, SEMA3A, FGF17, IL17RD, DUSP6, SPRY4, FLRT3, NELF, FEZF1, and CCDC141 (3).
Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations
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