F2

coagulation factor II, thrombin
OMIM: 176930, Gene2Phenotype

8 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 8 panels
Green F2 in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.43	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes {Pregnancy loss, recurrent, susceptibility to, 2} 614390 AD {Stroke, ischemic, susceptibility to} 601367 Mu Dysprothrombinemia 613679 AR Hypoprothrombinemia 613679 AR Thrombophilia due to thrombin defect 188050 AD Tags 5'UTR
Green F2 in Mendeliome Version 1.1891	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes {Pregnancy loss, recurrent, susceptibility to, 2} 614390 AD {Stroke, ischemic, susceptibility to} 601367 Mu Dysprothrombinemia 613679 AR Hypoprothrombinemia 613679 AR Thrombophilia due to thrombin defect 188050 AD Tags 5'UTR
Green F2 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Dysprothrombinemia, 613679 (3)
Green F2 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes Prothrombin deficiency
Green F2 in Prepair 1000+ Level 2: Screening Version 1.9	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Dysprothrombinaemia, 613679 Hypoprothrombinaemia (MIM#613679)
Red F2 in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category A gene BeginNGS Phenotypes Dysprothrombinemia MIM#613679 Hypoprothrombinemia MIM#613679 Thrombophilia due to thrombin defect MIM#188050
Green F2 in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes {Pregnancy loss, recurrent, susceptibility to, 2} 614390 AD Dysprothrombinemia 613679 AR Hypoprothrombinemia 613679 AR Thrombophilia due to thrombin defect 188050 AD {Stroke, ischemic, susceptibility to} 601367 Mu
Green F2 in Prepair 500+ Level 2: Screening Version 1.1	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Hypoprothrombinaemia (MIM#613679) Dysprothrombinaemia, 613679