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FGA - fibrinogen alpha chain

Synonym(s) :
Previous symbols and names : fibrinogen, A alpha polypeptide
Type : gene with protein product
Chromosomal location : 4q31.3
OMIM: 134820
HGNC: 3661
UniProtKB: P02671
Genatlas: FGA
GenCC: FGA
Ensembl: ENSG00000171560
IUPHAR-DB: -
Reactome: P02671
LOVD: FGA

Diseases list

Disease-causing germline mutation(s) in AFib amyloidosis ORPHA:93562
Disease-causing germline mutation(s) in Familial afibrinogenemia ORPHA:98880
Disease-causing germline mutation(s) in Familial dysfibrinogenemia ORPHA:98881
Disease-causing germline mutation(s) in Familial hypodysfibrinogenemia ORPHA:248408
Disease-causing germline mutation(s) in Familial hypofibrinogenemia ORPHA:101041

: Assessed

Additional information

Patient-centred resources for this gene

Diagnostic tests (98)

Research activities on this gene

Specialised Social Services

Eurordis directory

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