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GENE - TERM ANNOTATION REPORT
20 Annotations Found.
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:28883570 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:22389686
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:8600246 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:15870199
PMID:16299065
PMID:17947292
PMID:18252712
PMID:19259132
PMID:21909106
PMID:25741868
PMID:28492532
PMID:8072530
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:11578445 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:16299065
PMID:25741868
PMID:28492532
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:11579151 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:11978762
PMID:15761120
PMID:16619239
PMID:25741868
PMID:28492532
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:13838419 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:17576681
PMID:25741868
PMID:28492532
PMID:31575699
PMID:36246952
PMID:9536098
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:28888450 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:25741868
PMID:26559391
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:11577901 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:18557729
PMID:22171659
PMID:22223606
PMID:23431077
PMID:25037630
PMID:25741868
PMID:28492532
PMID:29888403
PMID:34189567
PMID:34508573
PMID:35925583
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:11577466 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:21415311
PMID:22223606
PMID:22403278
PMID:25741868
PMID:28492532
PMID:34189567
PMID:34508573
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:28891733 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:28492532
PMID:36445700
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:11578773 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:17018561
PMID:19190809
PMID:19297022
PMID:23852337
PMID:25741868
PMID:28492532
PMID:29888403
PMID:34189567
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:28886938 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:25741868
PMID:26501415
PMID:28492532
PMID:34508573
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:11579569 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:25741868
PMID:28492532
PMID:34508573
PMID:35925583
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:28880889 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:25741868
PMID:26501415
PMID:27718086
PMID:28492532
PMID:28941939
PMID:29500241
PMID:29888403
PMID:34260947
PMID:34508573
PMID:36445700
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:14398950 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:17599974
PMID:20203157
PMID:22456601
PMID:25741868
PMID:25814826
PMID:28492532
PMID:30560448
PMID:33519811
PMID:34189567
PMID:34508573
PMID:35925583
PMID:37369098
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:8600252 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:11158219
PMID:11170895
PMID:12424708
PMID:12697737
PMID:16338962
PMID:16601698
PMID:17018561
PMID:18235085
PMID:19454698
PMID:19633317
PMID:20016463
PMID:20059470
PMID:21317894
PMID:22019782
PMID:22410797
PMID:23431077
PMID:23685748
PMID:24036949
PMID:24036952
PMID:24498017
PMID:25087612
PMID:25741868
PMID:25814826
PMID:25880396
PMID:26215151
PMID:26376859
PMID:26691988
PMID:26826462
PMID:28011711
PMID:28859202
PMID:29410599
PMID:29500241
PMID:29888403
PMID:30674459
PMID:31447099
PMID:31589614
PMID:34169201
PMID:34189567
PMID:34508573
PMID:34748552
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:11577740|RGD:11578407|RGD:11578929|RGD:11579089|RGD:11579130|RGD:11579234|RGD:11582576|RGD:11584212|RGD:11585723|RGD:11586326|RGD:11587228|RGD:11651444|RGD:28882079 (Homo sapiens)
&
RGD:11577740|RGD:11578407|RGD:11578929|RGD:11579089|RGD:11579130|RGD:11579234|RGD:11582576|RGD:11584212|RGD:11585723|RGD:11586326|RGD:11587228|RGD:11651444|RGD:28882079 (Homo sapiens)
&
RGD:11577740|RGD:11578407|RGD:11578929|RGD:11579089|RGD:11579130|RGD:11579234|RGD:11582576|RGD:11584212|RGD:11585723|RGD:11586326|RGD:11587228|RGD:11651444|RGD:28882079 (Homo sapiens)
&
RGD:11577740|RGD:11578407|RGD:11578929|RGD:11579089|RGD:11579130|RGD:11579234|RGD:11582576|RGD:11584212|RGD:11585723|RGD:11586326|RGD:11587228|RGD:11651444|RGD:28882079 (Homo sapiens)
&
RGD:11577740|RGD:11578407|RGD:11578929|RGD:11579089|RGD:11579130|RGD:11579234|RGD:11582576|RGD:11584212|RGD:11585723|RGD:11586326|RGD:11587228|RGD:11651444|RGD:28882079 (Homo sapiens)
&
RGD:11577740|RGD:11578407|RGD:11578929|RGD:11579089|RGD:11579130|RGD:11579234|RGD:11582576|RGD:11584212|RGD:11585723|RGD:11586326|RGD:11587228|RGD:11651444|RGD:28882079 (Homo sapiens)
&
RGD:11577740|RGD:11578407|RGD:11578929|RGD:11579089|RGD:11579130|RGD:11579234|RGD:11582576|RGD:11584212|RGD:11585723|RGD:11586326|RGD:11587228|RGD:11651444|RGD:28882079 (Homo sapiens)
&
RGD:11577740|RGD:11578407|RGD:11578929|RGD:11579089|RGD:11579130|RGD:11579234|RGD:11582576|RGD:11584212|RGD:11585723|RGD:11586326|RGD:11587228|RGD:11651444|RGD:28882079 (Homo sapiens)
&
RGD:11577740|RGD:11578407|RGD:11578929|RGD:11579089|RGD:11579130|RGD:11579234|RGD:11582576|RGD:11584212|RGD:11585723|RGD:11586326|RGD:11587228|RGD:11651444|RGD:28882079 (Homo sapiens)
&
RGD:11577740|RGD:11578407|RGD:11578929|RGD:11579089|RGD:11579130|RGD:11579234|RGD:11582576|RGD:11584212|RGD:11585723|RGD:11586326|RGD:11587228|RGD:11651444|RGD:28882079 (Homo sapiens)
&
RGD:11577740|RGD:11578407|RGD:11578929|RGD:11579089|RGD:11579130|RGD:11579234|RGD:11582576|RGD:11584212|RGD:11585723|RGD:11586326|RGD:11587228|RGD:11651444|RGD:28882079 (Homo sapiens)
&
RGD:11577740|RGD:11578407|RGD:11578929|RGD:11579089|RGD:11579130|RGD:11579234|RGD:11582576|RGD:11584212|RGD:11585723|RGD:11586326|RGD:11587228|RGD:11651444|RGD:28882079 (Homo sapiens)
&
RGD:11577740|RGD:11578407|RGD:11578929|RGD:11579089|RGD:11579130|RGD:11579234|RGD:11582576|RGD:11584212|RGD:11585723|RGD:11586326|RGD:11587228|RGD:11651444|RGD:28882079 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:25741868
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:28882745 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:25443527
PMID:25741868
PMID:28492532
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
&
RGD:11577451|RGD:11577465|RGD:11577613|RGD:11577667|RGD:11577723|RGD:11577760|RGD:11577912|RGD:11577993|RGD:11577999|RGD:11578043|RGD:11578088|RGD:11578154|RGD:11578155|RGD:11578270|RGD:11578322|RGD:11578486|RGD:11578510|RGD:11578649|RGD:11578922|RGD:11578974|RGD:11579075|RGD:11579131|RGD:11579188|RGD:11579444|RGD:11579866|RGD:11582242|RGD:13481111|RGD:28887595|RGD:28891218|RGD:28896152 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:25741868
PMID:28492532
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
&
RGD:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
&
RGD:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
&
RGD:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
&
RGD:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
&
RGD:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
&
RGD:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
&
RGD:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
&
RGD:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
&
RGD:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
&
RGD:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
&
RGD:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
&
RGD:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
&
RGD:11579420|RGD:11582524|RGD:11583104|RGD:11588344|RGD:11646403|RGD:11649175|RGD:11651396|RGD:28878266|RGD:28882084|RGD:28886644|RGD:28887239|RGD:28887893|RGD:28888760|RGD:28892032 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
An association has been curated linking
CFH
and
C3 Glomerulopathy 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:11577459|RGD:11578419|RGD:11579368|RGD:11579565|RGD:11648951|RGD:28882754|RGD:28886300|RGD:28891228|RGD:28892594 (Homo sapiens)
&
RGD:11577459|RGD:11578419|RGD:11579368|RGD:11579565|RGD:11648951|RGD:28882754|RGD:28886300|RGD:28891228|RGD:28892594 (Homo sapiens)
&
RGD:11577459|RGD:11578419|RGD:11579368|RGD:11579565|RGD:11648951|RGD:28882754|RGD:28886300|RGD:28891228|RGD:28892594 (Homo sapiens)
&
RGD:11577459|RGD:11578419|RGD:11579368|RGD:11579565|RGD:11648951|RGD:28882754|RGD:28886300|RGD:28891228|RGD:28892594 (Homo sapiens)
&
RGD:11577459|RGD:11578419|RGD:11579368|RGD:11579565|RGD:11648951|RGD:28882754|RGD:28886300|RGD:28891228|RGD:28892594 (Homo sapiens)
&
RGD:11577459|RGD:11578419|RGD:11579368|RGD:11579565|RGD:11648951|RGD:28882754|RGD:28886300|RGD:28891228|RGD:28892594 (Homo sapiens)
&
RGD:11577459|RGD:11578419|RGD:11579368|RGD:11579565|RGD:11648951|RGD:28882754|RGD:28886300|RGD:28891228|RGD:28892594 (Homo sapiens)
&
RGD:11577459|RGD:11578419|RGD:11579368|RGD:11579565|RGD:11648951|RGD:28882754|RGD:28886300|RGD:28891228|RGD:28892594 (Homo sapiens)
&
RGD:11577459|RGD:11578419|RGD:11579368|RGD:11579565|RGD:11648951|RGD:28882754|RGD:28886300|RGD:28891228|RGD:28892594 (Homo sapiens)
2
RGD objects have been annotated to
C3 Glomerulopathy 3
(DOID:9008867)
60
papers in RGD have been used to annotate
CFH
Curation Notes: ClinVar Annotator: match by term: CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II
Original References(s):
PMID:28492532
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