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Hypogonadotropic hypogonadism (GMS) v2.5 PLXNA3 Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: PLXNA3.
Hypogonadotropic hypogonadism (GMS) v2.5 PLXNA3 Catherine Snow Tag Q3_22_rating was removed from gene: PLXNA3.
Hypogonadotropic hypogonadism (GMS) v2.5 PLXNA3 Catherine Snow commented on gene: PLXNA3
Hypogonadotropic hypogonadism (GMS) v2.4 PLXNA3 Catherine Snow Source Expert Review Green was added to PLXNA3.
Source NHS GMS was added to PLXNA3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Hypogonadotropic hypogonadism (GMS) v1.54 PLXNA3 Ivone Leong Tag Q3_22_rating tag was added to gene: PLXNA3.
Hypogonadotropic hypogonadism (GMS) v1.54 PLXNA3 Ivone Leong Classified gene: PLXNA3 as Amber List (moderate evidence)
Hypogonadotropic hypogonadism (GMS) v1.54 PLXNA3 Ivone Leong Added comment: Comment on list classification: New gene added by Zornitza Stark (Australian Genomics). This gene is not associated with any phenotypes in OMIM or Gene2Phenotype. Based on the expert review there is sufficient evidence to support a gene-disease association. This gene should be rated Green at the next review.
Hypogonadotropic hypogonadism (GMS) v1.54 PLXNA3 Ivone Leong Gene: plxna3 has been classified as Amber List (Moderate Evidence).
Hypogonadotropic hypogonadism (GMS) v1.52 PLXNA3 Ivone Leong Phenotypes for gene: PLXNA3 were changed from Hypogonadotropic hypogonadism to Hypogonadotropic hypogonadism, MONDO:0018555
Hypogonadotropic hypogonadism (GMS) v1.43 PLXNA3 Zornitza Stark gene: PLXNA3 was added
gene: PLXNA3 was added to Hypogonadotropic hypogonadism idiopathic. Sources: Literature
Mode of inheritance for gene: PLXNA3 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Publications for gene: PLXNA3 were set to 33495532
Phenotypes for gene: PLXNA3 were set to Hypogonadotropic hypogonadism
Review for gene: PLXNA3 was set to GREEN
Added comment: Screened 216 patients with Idiopathic hypogonadotropic hypogonadism by exome sequencing. Identified 7 individuals from 5 families with hemizygous PLXNA3 missense variants.
In 2 of the kindreds, there was at least one more gene known to be associated with IHH (oligogenecity). Data provided with evidence that PLXNA3, a key component of the SEMA3F holoreceptor complex,31 is expressed by the human GnRH and olfactory/vomeronasal systems. S646P variant showed PLXNA3 localization exclusively in the ER, indicating that the variant S646P disrupts cell surface localization of PLXNA3.
Sources: Literature