MNS1

meiosis specific nuclear structural 1
OMIM: 610766, Gene2Phenotype

3 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Amber MNS1 in Laterality disorders and isomerism Level 2: Respiratory Version 4.10 Latest signed off version: v4.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Heterotaxy, visceral, 9, autosomal, with male infertility, OMIM: 618948 situs inversus, MONDO:0010029 Tags Q1_26_promote_green Q1_26_NHS_review Q1_26_expert_review
Red MNS1 in Respiratory ciliopathies including non-CF bronchiectasis Level 2: Respiratory Version 4.55 Latest signed off version: v4.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources ClinGen Phenotypes Heterotaxy, visceral, 9, autosomal, with male infertility, OMIM:618948 Tags disputed
Amber MNS1 in Fetal anomalies Level 2: Fetal (including NIPD) Version 6.140 Latest signed off version: v6.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources NHS GMS Expert Review Amber Phenotypes Heterotaxy, visceral, 9, autosomal, with male infertility, OMIM:618948