WT1

Wilms tumor 1
OMIM: 607102, Gene2Phenotype

16 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 16 panels
Green WT1 in Congenital diaphragmatic hernia Level 2: Dysmorphic and congenital abnormality syndromes Version 1.14	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Denys-Drash syndrome, MIM# 194080
Green WT1 in Differences of Sex Development Level 2: Dysmorphic and congenital abnormality syndromes Version 0.293	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green WT1 in Incidentalome Version 0.301	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Denys-Drash syndrome, MIM# 194080 Frasier syndrome, MIM#136680 Wilms tumor, type 1, MIM#194070 Nephrotic syndrome, type 4, MIM#256370
Green WT1 in Proteinuria Level 2: Renal and urinary tract disorders Version 0.225 Component of the following Super Panels: Kidneyome_SuperPanel Renal Glomerular Disease_SuperPanel	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green WT1 in Cancer Predisposition_Paediatric Level 2: Cancer Version 0.131	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green WT1 in Additional findings_Adult Level 2: Screening Version 0.166	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Wilms' tumor MIM#194070
Green WT1 in Wilms Tumour Predisposition Level 2: Cancer predisposition Version 0.39	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Red WT1 in CGC_86 Version 0.2	review	Other	Sources CGC_86 Phenotypes Wilms tumor 1
Red WT1 in NCGC Version 0.2	review	Other	Sources NCGC Phenotypes Wilms tumor 1
Red WT1 in TCGA_PANCAN_2018 Version 0.2	review	Other	Sources TCGA_PANCAN_2018 Phenotypes Wilms tumor 1
Green WT1 in Primary Ovarian Insufficiency_Premature Ovarian Failure Level 3: Gonadal and sex development disorders Level 2: Endocrine disorders Version 0.328	review	Not set	Sources Expert Review Green Royal Melbourne Hospital
Amber WT1 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber BabySeq Category B gene BabySeq Category A gene Phenotypes Frasier syndrome Denys-Drash syndrome Wilms tumor, type 1
Red WT1 in Incidentalome_PREGEN_DRAFT Version 0.43	review	Unknown	Sources Expert Review Red NSW Health Pathology
Green WT1 in Fetal anomalies Version 1.255	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Victorian Clinical Genetics Services Phenotypes Denys-Drash syndrome, MIM# 194080 Frasier syndrome, MIM#136680
Green WT1 in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green BabySeq Category A gene BabySeq Category B gene Phenotypes Wilms tumor, type 1, MIM#194070 Tags cancer treatable
Green WT1 in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Phenotypes Wilms' tumor MIM#194070