FOXP3

forkhead box P3
OMIM: 300292, Gene2Phenotype

14 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 14 panels
Green FOXP3 in Vasculitis Level 2: Immunological disorders Version 0.82	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Red FOXP3 in Cataract Level 2: Ophthalmological disorders Version 0.366	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, 304790
Green FOXP3 in Congenital Diarrhoea Level 2: Gastroenterological disorders Version 1.13	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked , MIM#304790 Tags treatable
Green FOXP3 in Hydrops fetalis Level 2: Dysmorphic and congenital abnormality syndromes Version 0.313	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, 304790
Green FOXP3 in Inflammatory bowel disease Level 2: Gastroenterological disorders Version 0.121 Component of the following Super Panels: Immunological disorders_SuperPanel	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green FOXP3 in Mendeliome Version 1.1891	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, 304790 Tags treatable
Green FOXP3 in Disorders of immune dysregulation Level 2: Immunological disorders Version 0.186 Component of the following Super Panels: Immunological disorders_SuperPanel	review	Unknown	Sources Melbourne Genomics Health Alliance Immunology Flagship Victorian Clinical Genetics Services Expert Review Green Tags treatable
Green FOXP3 in Immune_markers_WTS_UMCCR Level 2: Cancer Version 0.75	review	Unknown	Sources Expert list Expert Review Green Tags umccr
Green FOXP3 in Monogenic Diabetes Level 2: Endocrine disorders Version 0.134 Component of the following Super Panels: Metabolic Disorders Superpanel	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green UKGTN Phenotypes immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome MONDO:0010580
Green FOXP3 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Mackenzie's Mission Phenotypes Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, 304790 (3)
Green FOXP3 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources BabySeq Category A gene Expert Review Green Phenotypes IPEX syndrome
Green FOXP3 in Fetal anomalies Version 1.255	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Genomics England PanelApp Phenotypes Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, 304790
Green FOXP3 in Prepair 1000+ Level 2: Screening Version 1.9	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Mackenzie's Mission Phenotypes Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, 304790 (3)
Green FOXP3 in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green BabySeq Category A gene BeginNGS Phenotypes IPEX syndrome, MIM#304790 Tags treatable immunological