WRAP53

WD repeat containing antisense to TP53
OMIM: 612661, ClinGen, DECIPHER

11 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 11 panels
Green WRAP53 in Haematological malignancies Level 2: Cancer susceptibility Version 0.148	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Curated sources Expert Review Green Victorian Clinical Genetics Services Phenotypes MDS, AML Bone marrow failure, macrocytosis Class: BM failure syndrome (typ AR) Skin, head and neck, and anogenital squamous cell cancers, Oral and GI squamous cell carcinoma Dyskeratosis congenita
Green WRAP53 in Bone Marrow Failure Level 2: Haematological disorders Version 2.9 Component of the following Super Panels: Immunological disorders_SuperPanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Dyskeratosis congenita, autosomal recessive 3, MIM# 613988
Green WRAP53 in Mendeliome Version 2.577	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Dyskeratosis congenita, autosomal recessive 3, MIM# 613988
Red WRAP53 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 2.145	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Expert list Phenotypes Dyskeratosis congenita, autosomal recessive 3 OMIM# 613988
Green WRAP53 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 1.0	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Dyskeratosis congenita, autosomal recessive 3, 613988 (3)
Green WRAP53 in Additional findings_Paediatric Level 2: Screening Version 1.1	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category C gene Phenotypes Dyskeratosis congenita, autosomal recessive 3, MIM# 613988
Red WRAP53 in Fetal anomalies Version 2.81	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Genomics England PanelApp Expert list Phenotypes Dyskeratosis congenita, autosomal recessive 3, OMIM #613988
Green WRAP53 in IBMDx study Version 1.2	1 review	Unknown	Sources Expert Review Green IBMDx Study Expert Review Green Victorian Clinical Genetics Services Phenotypes Dyskeratosis congenita, autosomal recessive 3, MIM# 613988
Green WRAP53 in Prepair 1000+ Level 2: Screening Version 3.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Dyskeratosis congenita, autosomal recessive 3, 613988 (3)
Red WRAP53 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 2.7	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category C gene Phenotypes Dyskeratosis congenita, autosomal recessive 3, MIM# 613988
Green WRAP53 in Hereditary Pigmentary Disorders Level 2: Dermatological disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Victorian Clinical Genetics Services Phenotypes Dyskeratosis congenita MONDO:0015780