the single-nucleotide polymorphism rs850807 which is putatively functional and linked with MAGEL2 and NDN Genetic variation in rs850807 was strongly and exclusively associated with the ideas of reference subscale of the schizophrenia spectrum which is best typified as paranoia
One candidate variant was located in an alpha helix of Necdin (NDN) phased to the paternally inherited allele. NDN is maternally imprinted within the 15q11.2 Prader-Willi Syndrome (PWS) region
rare variant of necdin (p.V318A) was described in a family with Kallmann syndrome Familial segregation and in vitro analysis suggested that this non-synonymous variant did not have a direct causative role in hypogonadism phenotype.
Not Associated with METABOLIC: Body Weight Regulation., Not Associated with METABOLIC: body mass., Observational study of gene-disease association. (HuGE Navigator)
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