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GENE - TERM ANNOTATION REPORT
1 Annotations Found.
An association has been curated linking
F2
and
prothrombin deficiency
in Chinchilla lanigera.
The association was
inferred from sequence orthology
(ISO)
The annotation was made from
RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred from sequence orthology with
F2 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
3
RGD objects have been annotated to
prothrombin deficiency
(DOID:2235)
2
papers in RGD have been used to annotate
F2
Curation Notes: ClinVar Annotator: match by term: Congenital factor II deficiency | ClinVar Annotator: match by term: Factor II deficiency
Original References(s):
PMID:10027711
PMID:10233438
PMID:10233439
PMID:10336270
PMID:10348710
PMID:10348711
PMID:10348712
PMID:10406905
PMID:10477778
PMID:10544935
PMID:11358905
PMID:11443298
PMID:11506076
PMID:11796466
PMID:11874997
PMID:11904676
PMID:13228032
PMID:14629473
PMID:15059842
PMID:15534175
PMID:16493002
PMID:16606808
PMID:19159930
PMID:19289024
PMID:19531787
PMID:19554541
PMID:19560233
PMID:19598065
PMID:19652888
PMID:20301327
PMID:21243428
PMID:21349849
PMID:2222810
PMID:23429074
PMID:24033266
PMID:2429850
PMID:25741868
PMID:27031503
PMID:2825773
PMID:28492532
PMID:28707429
PMID:30297698
PMID:31064749
PMID:34110897
PMID:34355501
PMID:6305407
PMID:6405779
PMID:7740448
PMID:8696333
PMID:8896550
PMID:8916933
PMID:9106528
PMID:9292507
PMID:9462220
PMID:9493607
PMID:9531249
PMID:9569177
PMID:9694698
PMID:9869612
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