TSPYL1

TSPY like 1
OMIM: 604714, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green TSPYL1 in Differences of Sex Development Level 2: Dysmorphic and congenital abnormality syndromes Version 0.293	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Sudden infant death with dysgenesis of the testes syndrome (MIM#608800) Tags disputed
Green TSPYL1 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Sudden infant death with dysgenesis of the testes syndrome (MIM#608800) sudden infant death-dysgenesis of the testes syndrome MONDO:0012124
Green TSPYL1 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.33 Component of the following Super Panels: Progressive Neurological Conditions	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Expert list Expert Review Green Victorian Clinical Genetics Services Phenotypes Sudden infant death with dysgenesis of the testes syndrome - 608800 sudden infant death-dysgenesis of the testes syndrome MONDO:0012124
Red TSPYL1 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Mackenzie's Mission Phenotypes Sudden infant death with dysgenesis of the testes syndrome, 608800 (3)
Red TSPYL1 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category C gene Phenotypes Sudden infant death with dysgenesis of the testes syndrome
Red TSPYL1 in Prepair 1000+ Level 2: Screening Version 1.9	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Mackenzie's Mission Phenotypes Sudden infant death with dysgenesis of the testes syndrome, 608800 (3)
Red TSPYL1 in BabyScreen+ newborn screening Level 2: Screening Version 1.114	review	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category C gene Expert Review Red Phenotypes Sudden infant death with dysgenesis of the testes syndrome