WT1:Ensemblv115

WT1 transcription factor
OMIM: 607102, ClinGen, DECIPHER

11 panels

Panel Reviews Mode of inheritance Details
11 panels

Green WT1 in Congenital diaphragmatic hernia


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green
Phenotypes
  • Denys-Drash syndrome, MIM# 194080

Green WT1 in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green
Phenotypes
  • Wilms tumor, MONDO:0006058
  • Wilms tumor 1, MONDO:0008679
  • Wilms tumor, type 1, MIM#194070
  • Denys-Drash syndrome, MIM#194080
  • Frasier syndrome, MIM#136680

Green WT1 in Incidentalome


Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green
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 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green
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 Cancer Predisposition_Paediatric


Level 2: Cancer
Version 1.0

0 reviews Unknown
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services

Green WT1 in Additional findings_Adult


Level 2: Screening
Version 2.0

0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Wilms' tumor MIM#194070

Green WT1 in Wilms Tumour Predisposition


Level 2: Cancer predisposition
Version 1.0

0 reviews Unknown
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services

Green WT1 in Primary Ovarian Insufficiency_Premature Ovarian Failure

Level 3: Gonadal and sex development disorders
Level 2: Endocrine disorders
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert List
Phenotypes
  • Primary ovarian failure, MONDO:0005387

Green WT1 in Fetal anomalies


Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Genomics England PanelApp
  • Expert Review Green
Phenotypes
  • Denys-Drash syndrome, MIM# 194080
  • Frasier syndrome, MIM#136680

Green WT1 in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • BabySeq Category B gene
  • BabySeq Category A gene
  • Expert Review Green
Phenotypes
  • Wilms tumor, type 1, MIM#194070
Tags
  • cancer
  • treatable

Green WT1 in Transplant Co-Morbidity


Level 2: Screening
Version 1.0

0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Wilms' tumor MIM#194070