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GENE - TERM ANNOTATION REPORT

RGD ID: 737209
Species: Homo sapiens
RGD Object: Gene
Symbol: FGA
Name: fibrinogen alpha chain
Acc ID: DOID:9003464
Term: Congenital Dysfibrinogenemia
Definition: A hereditary, usually autosomal dominant disorder that affects the quality of circulating FIBRINOGEN. About half of patients are asymptomatic, and half have an increased tendency for bleeding, THROMBOSIS, or both.
Definition Source(s): MESH:C562727
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
FGA IAGP 7240710OMIM  
FGA EXP 11554173CTDCTD Direct Evidence: marker/mechanism 
FGA IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenitalPMID:25741868
FGA IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenitalPMID:25741868 PMID:28492532
FGA IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenitalPMID:10887149 PMID:25741868 PMID:26763372 PMID:28492532
FGA IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenitalPMID:16651864 PMID:19468208 PMID:25741868
FGA IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenitalPMID:25741868 PMID:31064749
FGA IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenitalPMID:15795544 PMID:23852822
FGA IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenitalPMID:25981141
FGA IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenitalPMID:10891444 PMID:9916133
FGA IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenital 
FGA IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenitalPMID:11435303 PMID:11460527 PMID:15009465 PMID:16846481 PMID:1912564 PMID:19923982 PMID:22967385 PMID:25741868 PMID:26676819 PMID:2738154 PMID:28101869 PMID:30332696 PMID:30349899 PMID:31924745 PMID:32877852 PMID:33477601 PMID:33807613 PMID:34275736 PMID:3667568 PMID:4082078 PMID:6667926 PMID:8140431 PMID:8457654
FGA IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: FIBRINOGEN AARHUS 1PMID:10605955 PMID:23852822 PMID:25320241 PMID:25741868 PMID:26006300 PMID:26577257 PMID:30856382 PMID:31064749 PMID:31314131
FGA IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: FIBRINOGEN CARACAS 2PMID:1675636 PMID:25741868
FGA IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenitalPMID:12050338 PMID:19109585 PMID:25741868 PMID:32660897 PMID:8113408 PMID:8944230
FGA IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenitalPMID:25741868 PMID:34355501 PMID:8473507 PMID:8636415
FGA IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenitalPMID:10891444 PMID:14615374 PMID:17576681 PMID:25741868 PMID:28492532 PMID:30349899 PMID:31064749 PMID:9536098
FGA IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Dysfibrinogenemia, congenitalPMID:17982313 PMID:22880226 PMID:25741868 PMID:25816717 PMID:2738154 PMID:27684817 PMID:28101869 PMID:30332696 PMID:31064749 PMID:32166693 PMID:32877852 PMID:3345340 PMID:33668986 PMID:34275736 PMID:3590111 PMID:3618591 PMID:4052020 PMID:6191801 PMID:7298640
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