ABCA1

ATP binding cassette subfamily A member 1
OMIM: 600046, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green ABCA1 in Mendeliome Version 1.3512	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Tangier disease, MIM# 205400 HDL deficiency, familial, 1, MIM# 604091 Tags somatic 5'UTR
Green ABCA1 in Dyslipidaemia Level 2: Endocrine disorders Version 0.46 Component of the following Super Panels: Metabolic Disorders Superpanel	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Tangier disease, MIM# 205400 HDL deficiency, familial, 1, MIM# 604091
Green ABCA1 in Hereditary Neuropathy - complex Level 2: Neurology and neurodevelopmental disorders Version 1.40 Component of the following Super Panels: Hereditary Neuropathy_CMT_IsolatedAndComplex Neuromuscular Superpanel Progressive Neurological Conditions	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Tangier Disease (MONDO:0008783 MIM#205400)
Green ABCA1 in Stroke Level 2: Neurology and neurodevelopmental disorders Version 1.28	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Green Literature Victorian Clinical Genetics Services Phenotypes Tangier disease MIM#205400
Green ABCA1 in Transplant Co-Morbidity Level 2: Screening Version 0.20	0 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes HDL deficiency, familial, 1, MIM# 604091 Tangier disease, MIM# 205400