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GENE - TERM ANNOTATION REPORT
27 Annotations Found.
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:41406732 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:25741868
PMID:33532864
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:21070305 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:24830959
PMID:26920127
PMID:28381550
PMID:28492532
PMID:29254190
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:13529494 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:24033266
PMID:25741868
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:243049775 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:31690835
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:21073939 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:24058621
PMID:24830959
PMID:25741868
PMID:25810436
PMID:26467025
PMID:28288174
PMID:28492532
PMID:28555925
PMID:32576985
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:8597585 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:10831588
PMID:10906158
PMID:11734858
PMID:21631963
PMID:23703872
PMID:23991001
PMID:25741868
PMID:25810436
PMID:26467025
PMID:28381550
PMID:28492532
PMID:31115572
PMID:32857947
PMID:9326936
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:8560012 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:11102542
PMID:25741868
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:41406236 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:28492532
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:151756507 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:24830959
PMID:25741868
PMID:28492532
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:21070309 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:21865213
PMID:28381550
PMID:28492532
PMID:31803959
PMID:31834604
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:38460525 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:10906158
PMID:24830959
PMID:25741868
PMID:26920127
PMID:28381550
PMID:28492532
PMID:29254190
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:13470863 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:17185149
PMID:24830959
PMID:25525159
PMID:25810436
PMID:26467025
PMID:26920127
PMID:28381550
PMID:28492532
PMID:29254190
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:150536485 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:21415153
PMID:24058621
PMID:24271511
PMID:24830959
PMID:25741868
PMID:28381550
PMID:28492532
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:8597584 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:15875219
PMID:24830959
PMID:25741868
PMID:28492532
PMID:31803959
PMID:33532864
PMID:9326936
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:8597588 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:15531551
PMID:16902263
PMID:17622951
PMID:24830959
PMID:24965226
PMID:25741868
PMID:26920127
PMID:28381550
PMID:28492532
PMID:29254190
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:11350682 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:24830959
PMID:25741868
PMID:26920127
PMID:28381550
PMID:28492532
PMID:29254190
PMID:31672324
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:405281692 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:25741916
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:13531146 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:24033266
PMID:25741868
PMID:28492532
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:10405791 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:24830959
PMID:25326637
PMID:25741868
PMID:26920127
PMID:28381550
PMID:28492532
PMID:29254190
PMID:31672324
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:38598741 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:20810575
PMID:24830959
PMID:25741868
PMID:26920127
PMID:28381550
PMID:28492532
PMID:29254190
PMID:30773290
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:8597583|RGD:8597586|RGD:8597587 (Homo sapiens)
&
RGD:8597583|RGD:8597586|RGD:8597587 (Homo sapiens)
&
RGD:8597583|RGD:8597586|RGD:8597587 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:9326936
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:13611927|RGD:21070306 (Homo sapiens)
&
RGD:13611927|RGD:21070306 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:24830959
PMID:25741868
PMID:26920127
PMID:28381550
PMID:28492532
PMID:29254190
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
&
RGD:13832036|RGD:14702794|RGD:14702797|RGD:150330637|RGD:150337429|RGD:150413718|RGD:150413727|RGD:150413910|RGD:150413913|RGD:150413918|RGD:150413925|RGD:150413997|RGD:150414001|RGD:150414172|RGD:150414175|RGD:150414178|RGD:151349582|RGD:151661852|RGD:155799038|RGD:21070308|RGD:38460521|RGD:401797562|RGD:401855544|RGD:8621369|RGD:8621370 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:25741868
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:11634331|RGD:21070310|RGD:21070312 (Homo sapiens)
&
RGD:11634331|RGD:21070310|RGD:21070312 (Homo sapiens)
&
RGD:11634331|RGD:21070310|RGD:21070312 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
&
RGD:13611924|RGD:150334401|RGD:15112192|RGD:15118452|RGD:15149768|RGD:15150253|RGD:15155693|RGD:15156855|RGD:151758508|RGD:151772527|RGD:15178677|RGD:15179940|RGD:151799764|RGD:151822326|RGD:151823769|RGD:151874829|RGD:151876955|RGD:151889605|RGD:15196702|RGD:15196815|RGD:152064914|RGD:152070822|RGD:152105945|RGD:152110992|RGD:152112257|RGD:152147877|RGD:152148457|RGD:152159501|RGD:38462826|RGD:38467297 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:25741868
PMID:28492532
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:12833145|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens)
&
RGD:12833145|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens)
&
RGD:12833145|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens)
&
RGD:12833145|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens)
&
RGD:12833145|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens)
&
RGD:12833145|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens)
&
RGD:12833145|RGD:13478768|RGD:13480045|RGD:13482451|RGD:13484771|RGD:13504217|RGD:13504279 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:24033266
PMID:25741868
PMID:26467025
PMID:28492532
An association has been curated linking
LOC106501713
and
Bartter disease type 3
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
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 by association of genotype and phenotype with
RGD:12838494|RGD:13481618|RGD:13808933 (Homo sapiens)
&
RGD:12838494|RGD:13481618|RGD:13808933 (Homo sapiens)
&
RGD:12838494|RGD:13481618|RGD:13808933 (Homo sapiens)
5
RGD objects have been annotated to
Bartter disease type 3
(DOID:0110144)
0
papers in RGD have been used to annotate
LOC106501713
Curation Notes: ClinVar Annotator: match by term: Bartter disease type 3
Original References(s):
PMID:25741868
PMID:26467025
PMID:28492532
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