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GENE - TERM ANNOTATION REPORT
RGD ID:
3075
Species:
Rattus norvegicus
RGD Object:
Gene
Symbol:
Mecp2
Name:
methyl CpG binding protein 2
Acc ID:
DOID:9004536
Term:
Rett Syndrome, Zappella Variant
Definition:
null
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)
Mecp2
ISO
MECP2 (Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Rett syndrome, zappella variant
PMID:10508514
PMID:10577905
PMID:10745042
PMID:10767337
PMID:10814718
PMID:10852707
PMID:10854091
PMID:10991688
PMID:11035019
PMID:11055878
PMID:11055898
PMID:11058114
PMID:11106359
PMID:11241840
PMID:11245712
PMID:11269512
PMID:11309679
PMID:11313756
PMID:11376998
PMID:11402105
PMID:11462237
PMID:11469283
PMID:11738866
PMID:11738879
PMID:11738883
PMID:11738885
PMID:11746022
PMID:11913567
PMID:1191367
PMID:11960578
PMID:12111643
PMID:12180070
PMID:12325033
PMID:12552569
PMID:12567420
PMID:12673788
PMID:12707946
PMID:12746406
PMID:12770674
PMID:12843318
PMID:12966523
PMID:14560307
PMID:15057977
PMID:15173251
PMID:15389714
PMID:15526954
PMID:15737703
PMID:16122633
PMID:16473305
PMID:16690727
PMID:16763963
PMID:16844334
PMID:17089071
PMID:17101771
PMID:17142618
PMID:17341617
PMID:17387578
PMID:17986102
PMID:18332345
PMID:18414213
PMID:18562141
PMID:18989701
PMID:19652677
PMID:19722030
PMID:19914908
PMID:20031356
PMID:20151026
PMID:20301670
PMID:21160487
PMID:21831886
PMID:21878110
PMID:21954873
PMID:21982064
PMID:22277191
PMID:22368975
PMID:22476991
PMID:22516699
PMID:23260135
PMID:23262346
PMID:23421866
PMID:23696494
PMID:23810759
PMID:23921973
PMID:25741868
PMID:25741916
PMID:26175308
PMID:26418480
PMID:26467025
PMID:26647311
PMID:26795593
PMID:26842955
PMID:26984561
PMID:27799067
PMID:27929079
PMID:28394482
PMID:28492532
PMID:29655203
PMID:29758562
PMID:30536762
PMID:32472557
PMID:34324427
PMID:34837432
PMID:4413922
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