SLC2A10

solute carrier family 2 member 10
OMIM: 606145, ClinGen, DECIPHER

15 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 15 panels
Green SLC2A10 in Vasculitis Level 2: Immunological disorders Version 0.86	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green SLC2A10 in Aortopathy_Connective Tissue Disorders Level 2: Cardiovascular disorders Version 1.86	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Arterial tortuosity syndrome MIM#208050
Green SLC2A10 in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.52	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Arterial tortuosity syndrome, MIM# 208050
Green SLC2A10 in Mendeliome Version 1.2302	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Arterial tortuosity syndrome, MIM# 208050
Red SLC2A10 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Expert list Phenotypes Arterial tortuosity syndrome OMIM #208050
Green SLC2A10 in Cutis Laxa Level 2: Dermatological disorders Version 1.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green GeneReviews Phenotypes Arterial tortuosity syndrome MIM#208050
Green SLC2A10 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Arterial tortuosity syndrome, 208050 (3)
Green SLC2A10 in Stroke Level 2: Neurology and neurodevelopmental disorders Version 1.16	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Arterial tortuosity syndrome 208050 Moyamoya disease
Green SLC2A10 in Cerebral vascular malformations Level 2: Neurology and neurodevelopmental disorders Version 1.0 Component of the following Super Panels: Progressive Neurological Conditions	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Genomics England PanelApp Expert Review Green Phenotypes 208050 Moyamoya disease Arterial tortuosity syndrome
Green SLC2A10 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes Arterial tortuosity syndrome
Green SLC2A10 in Fetal anomalies Version 1.313	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Expert list Phenotypes Arterial tortuosity syndrome, MIM# 208050
Green SLC2A10 in Prepair 1000+ Level 2: Screening Version 1.1566	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Arterial tortuosity syndrome, 208050 (3)
Red SLC2A10 in BabyScreen+ newborn screening Level 2: Screening Version 1.116	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category A gene Phenotypes Arterial tortuosity syndrome MIM#208050
Green SLC2A10 in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Arterial tortuosity syndrome, MIM# 208050
Green SLC2A10 in Vitamin metabolism disorders Level 2: Metabolic disorders Version 1.7 Component of the following Super Panels: Metabolic Disorders Superpanel	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Phenotypes Arterial tortuosity syndrome MONDO:0008818 Other disorders of vitamin metabolism