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GENE - TERM ANNOTATION REPORT
RGD ID:
628843
Species:
Rattus norvegicus
RGD Object:
Gene
Symbol:
Mfn2
Name:
mitofusin 2
Acc ID:
DOID:630
Term:
genetic disease
Definition:
A disease that has_material_basis_in genetic variations in the human genome. (DO)
Definition Source(s):
http://ghr.nlm.nih.gov/
"DO" "DO"
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 Symbol
Qualifier
Evidence
With
Reference
Source
Notes
Original Reference(s)
Mfn2
ISO
MFN2 (Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:15064763
PMID:15549395
PMID:16043786
PMID:16437557
PMID:16714318
PMID:16762064
PMID:16835246
PMID:17215403
PMID:17296794
PMID:17437620
PMID:17444508
PMID:17576681
PMID:18316077
PMID:18425620
PMID:18458227
PMID:18946002
PMID:18957892
PMID:18996695
PMID:19350291
PMID:19618221
PMID:19812251
PMID:19889647
PMID:20008656
PMID:20335458
PMID:20350294
PMID:20418531
PMID:20482598
PMID:21258814
PMID:21285398
PMID:21326314
PMID:21508331
PMID:21519004
PMID:21531138
PMID:21576112
PMID:21707411
PMID:21715711
PMID:21840889
PMID:22442078
PMID:22492563
PMID:22851605
PMID:22926664
PMID:22957060
PMID:23456260
PMID:23615052
PMID:23781337
PMID:23806086
PMID:24033266
PMID:24088041
PMID:24126688
PMID:24450158
PMID:24473995
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PMID:24627108
PMID:24819634
PMID:24862862
PMID:24863639
PMID:24957169
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PMID:25403865
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PMID:26114802
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PMID:26147798
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PMID:26307494
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PMID:26392352
PMID:26467025
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PMID:26686600
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PMID:30659145
PMID:30882371
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PMID:31186069
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PMID:31372974
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PMID:31640251
PMID:31664033
PMID:31673878
PMID:31701603
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PMID:32376792
PMID:32399692
PMID:32657593
PMID:33415332
PMID:33475540
PMID:33502018
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PMID:34060689
PMID:34103343
PMID:34193129
PMID:34232518
PMID:34366782
PMID:34721278
PMID:35418194
PMID:35922214
PMID:35936615
PMID:35938991
PMID:36964972
PMID:37797217
PMID:8406488
PMID:9409358
PMID:9536098
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