CYP1B1

cytochrome P450 family 1 subfamily B member 1
OMIM: 601771, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green CYP1B1 in Eye Anterior Segment Abnormalities Level 2: Ophthalmological disorders Version 1.15	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Anterior segment dysgenesis 6, multiple subtypes, MIM# 617315
Green CYP1B1 in Glaucoma congenital Level 2: Ophthalmological disorders Version 1.9	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, MIM# 231300
Green CYP1B1 in Mendeliome Version 1.3512	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Anterior segment dysgenesis 6, multiple subtypes, 617315 Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, 231300
Green CYP1B1 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.110	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, 231300 (3)
Green CYP1B1 in Fetal anomalies Version 1.465	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes Anterior segment dysgenesis 6, multiple subtypes, MIM# 617315 Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, MIM# 231300
Green CYP1B1 in Prepair 1000+ Level 2: Screening Version 2.14	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, MIM#231300 Anterior segment dysgenesis 6, multiple subtypes, MIM#617315
Green CYP1B1 in Prepair 500+ Level 2: Screening Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Anterior segment dysgenesis 6, multiple subtypes, MIM#617315