TEK

TEK receptor tyrosine kinase
OMIM: 600221, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green TEK in Glaucoma congenital Level 2: Ophthalmological disorders Version 1.9	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Glaucoma 3, primary congenital, E, MIM# 617272
Green TEK in Mendeliome Version 1.1902	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Glaucoma 3, primary congenital, E, MIM# 617272 Venous malformations, multiple cutaneous and mucosal, MIM# 600195
Green TEK in Vascular Malformations_Germline Level 2: Cardiovascular disorders Version 1.11 Component of the following Super Panels: Vascular Malformations SuperPanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Venous malformations, multiple cutaneous and mucosal 600195
Red TEK in Cerebral vascular malformations Level 2: Neurology and neurodevelopmental disorders Version 0.39 Component of the following Super Panels: Progressive Neurological Conditions	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Genomics England PanelApp Expert Review Red Phenotypes Venous malformations, multiple cutaneous and mucosal, 600195 Multiple Cutaneous and Mucosal Venous Malformations
Green TEK in Vascular Malformations_Somatic Level 2: Cardiovascular disorders Version 1.13 Component of the following Super Panels: Vascular Malformations SuperPanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Phenotypes Venous malformations, multiple cutaneous and mucosal (600195) Blue rubber bleb naevus syndrome Sporadic multifocal vascular malformations
Amber TEK in Mosaic skin disorders Level 2: Dermatological disorders Version 1.12 Component of the following Super Panels: Vascular Malformations SuperPanel	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Amber Genomics England PanelApp NHS GMS Phenotypes Venous malformations, multiple cutaneous and mucosal, 600195
Red TEK in Fetal anomalies Version 1.255	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Red Genomics England PanelApp Phenotypes Glaucoma 3, primary congenital, E (MIM#617272) Venous malformations, multiple cutaneous and mucosal (MIM#600195)