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GENE - TERM ANNOTATION REPORT
1 Annotations Found.
An association has been curated linking
CUNH17orf107
and
congenital myasthenic syndrome
in Ictidomys tridecemlineatus.
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
C17orf107 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
183
RGD objects have been annotated to
congenital myasthenic syndrome
(DOID:3635)
0
papers in RGD have been used to annotate
CUNH17orf107
Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome | ClinVar Annotator: match by term: Myasthenic syndrome, slow-channel congenital
Original References(s):
PMID:10496269
PMID:10514102
PMID:10534268
PMID:12141316
PMID:12356851
PMID:12417530
PMID:12536367
PMID:14532324
PMID:15322984
PMID:15367858
PMID:16199547
PMID:17576681
PMID:17878953
PMID:18414213
PMID:19153382
PMID:19544078
PMID:20157724
PMID:20301347
PMID:20562457
PMID:21150643
PMID:21940170
PMID:22382357
PMID:22678886
PMID:24033266
PMID:24295813
PMID:25326635
PMID:25741868
PMID:26284228
PMID:26467025
PMID:27634344
PMID:27717316
PMID:28464723
PMID:28492532
PMID:29054425
PMID:29189923
PMID:29383513
PMID:31773638
PMID:31980526
PMID:32727330
PMID:36099689
PMID:8755487
PMID:9097970
PMID:9158150
PMID:9536098
PMID:9539130
PMID:9668239
PMID:9708546
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