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GENE - TERM ANNOTATION REPORT
53 Annotations Found.
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
The annotation was made from
Bachmann-Gagescu R, etal., J Med Genet. 2012 Feb;49(2):126-37. doi: 10.1136/jmedgenet-2011-100552.
5
additional annotations were made from
Bachmann-Gagescu R, etal., J Med Genet. 2012 Feb;49(2):126-37. doi: 10.1136/jmedgenet-2011-100552.
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: DNA:mutations: :multiple
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
The annotation was made from
Bachmann-Gagescu R, etal., J Med Genet. 2012 Feb;49(2):126-37. doi: 10.1136/jmedgenet-2011-100552.
5
additional annotations were made from
Bachmann-Gagescu R, etal., J Med Genet. 2012 Feb;49(2):126-37. doi: 10.1136/jmedgenet-2011-100552.
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Qualifier: no_association
Curation Notes: DNA:mutations: :multiple
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448773 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:22241855
PMID:25741868
PMID:26092869
PMID:28492532
PMID:30055837
PMID:33502066
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
The annotation was made from
Noor A, etal., Am J Hum Genet. 2008 Nov;83(5):656.
2
additional annotations were made from
Noor A, etal., Am J Hum Genet. 2008 Nov;83(5):656.
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: DNA:splice-site mutation:intron:IVS19+1G>C (human)
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448802 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:25741868
PMID:26092869
PMID:26310553
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8617044 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:16199547
PMID:19466712
PMID:19777577
PMID:25741868
PMID:26092869
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8555799 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:18387594
PMID:18950740
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448737 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:26092869
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8595124 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:19574260
PMID:22241855
PMID:26092869
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448718 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:19777577
PMID:26092869
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
in Homo sapiens.
The association was
inferred by association of genotype and phenotype
(IAGP)
The annotation was made from
OMIM Disease Annotation Pipeline
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10406539 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:19777577
PMID:25741868
PMID:26673778
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8602372 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9/15, digenic
Original References(s):
PMID:22246503
PMID:25741868
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8591119 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:25741868
PMID:26467025
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8591117 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:18414213
PMID:25741868
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8591111 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:18414213
PMID:21068128
PMID:21370303
PMID:22241855
PMID:25741868
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10049072 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:21370303
PMID:22241855
PMID:25741868
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448771 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:19777577
PMID:22241855
PMID:22425360
PMID:23012439
PMID:25741868
PMID:26092869
PMID:26477546
PMID:26485645
PMID:26673778
PMID:28492532
PMID:29146704
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8617033 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:19466712
PMID:19777577
PMID:25741868
PMID:27894351
PMID:28492532
PMID:30202406
PMID:31130284
PMID:33486889
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448776 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:17576681
PMID:18950740
PMID:25741868
PMID:26092869
PMID:28492532
PMID:38259611
PMID:9536098
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8595120 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:18950740
PMID:25741868
PMID:26092869
PMID:28492532
PMID:29620724
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
&
RGD:10050408|RGD:10050409|RGD:10050480|RGD:10052980|RGD:10405447|RGD:10405517|RGD:10408104|RGD:11347843|RGD:11349155|RGD:11349891|RGD:11350040|RGD:11549744|RGD:11550703|RGD:11551461|RGD:11580349|RGD:11590920|RGD:11591085|RGD:11592228|RGD:11594416|RGD:11638997|RGD:11640242|RGD:11643026|RGD:11652247|RGD:11653254|RGD:126773852|RGD:12913703|RGD:13515899|RGD:13540215|RGD:13837643|RGD:14695775|RGD:151349626|RGD:151768671|RGD:26887463|RGD:28869898|RGD:38491631|RGD:8591112|RGD:8591120|RGD:8591123|RGD:8591130|RGD:8591131|RGD:8640450|RGD:9692752|RGD:9692754 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:25741868
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448715 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:19777577
PMID:25741868
PMID:26092869
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
&
RGD:10045205|RGD:11544025|RGD:11550263|RGD:126741088|RGD:127238176|RGD:13612097|RGD:13703288|RGD:13827673|RGD:14695870|RGD:150408055|RGD:150408425|RGD:150452502|RGD:150530930|RGD:150532051|RGD:151349733|RGD:155795141|RGD:156436043|RGD:34891614|RGD:34891615|RGD:401940226|RGD:405280623|RGD:40814892|RGD:8591113|RGD:8591114|RGD:8591115|RGD:8591116|RGD:8591118|RGD:8591122|RGD:8591124|RGD:8591126 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:25741868
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:26903765 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:16199547
PMID:19777577
PMID:25741868
PMID:28492532
PMID:34906502
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448709 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:18950740
PMID:19777577
PMID:22241855
PMID:25741868
PMID:26092869
PMID:27081510
PMID:27082236
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8617041 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:19777577
PMID:21068128
PMID:24706459
PMID:25741868
PMID:26092869
PMID:26729329
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448799 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:17576681
PMID:26092869
PMID:28492532
PMID:9536098
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8617035 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:18950740
PMID:19466712
PMID:19574260
PMID:19777577
PMID:22241855
PMID:25741868
PMID:26092869
PMID:28125082
PMID:28492532
PMID:32488064
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8595123 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9/15, digenic
Original References(s):
PMID:19574260
PMID:19777577
PMID:22246503
PMID:25741868
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8617036 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:19466712
PMID:19777577
PMID:25741868
PMID:26092869
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448688 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:21068128
PMID:22241855
PMID:26092869
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:13811427 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:23692786
PMID:25741868
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448758 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:17576681
PMID:22241855
PMID:26092869
PMID:28492532
PMID:9536098
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:150530851 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:19777577
PMID:25741868
PMID:28492532
PMID:30091983
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:14706114 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:19777577
PMID:25741868
PMID:27848944
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448699 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:22241855
PMID:25741868
PMID:26092869
PMID:27894351
PMID:28492532
PMID:34645488
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
in Homo sapiens.
The association was
inferred from experiment
(EXP)
The annotation was made from
RGD automated import pipeline for CTD gene-to-disease annotations
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: CTD Direct Evidence: marker/mechanism
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:9692751 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:16199547
PMID:19777577
PMID:26092869
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
&
RGD:11345769|RGD:11580612|RGD:11585400|RGD:11585884|RGD:11589492|RGD:11589688|RGD:11591010|RGD:11591781|RGD:11592215|RGD:11593587|RGD:11593598|RGD:11595405|RGD:11640877|RGD:11642562|RGD:11646130|RGD:11646340|RGD:11646775|RGD:11649076|RGD:11650880|RGD:11651865|RGD:11656908|RGD:11657871|RGD:11659467|RGD:12836986|RGD:12898829|RGD:12900473|RGD:12913204|RGD:13519334|RGD:13524038|RGD:13835530|RGD:13837586|RGD:14730546|RGD:26897165|RGD:28869398|RGD:28872790|RGD:28876208|RGD:28880720|RGD:28881398|RGD:28883561|RGD:28903673|RGD:9692755 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448741 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:22241855
PMID:26092869
PMID:28125082
PMID:28497568
PMID:29146704
PMID:30055837
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:28871853 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:19466712
PMID:25741868
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8595122 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:18950740
PMID:19777577
PMID:25525159
PMID:25741868
PMID:26092869
PMID:27959436
PMID:28492532
PMID:31618753
PMID:3631907
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448796 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:22241855
PMID:25741868
PMID:26092869
PMID:28492532
PMID:8253763
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448778 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:19777577
PMID:22241855
PMID:26092869
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10405509 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:18414213
PMID:19777577
PMID:25741868
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:8595121 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:18950740
PMID:19574260
PMID:25741868
PMID:26092869
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10405503|RGD:8591110 (Homo sapiens)
&
RGD:10405503|RGD:8591110 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:22241855
PMID:25741868
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448721|RGD:10448787 (Homo sapiens)
&
RGD:10448721|RGD:10448787 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:22241855
PMID:26092869
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
&
RGD:11595376|RGD:11644974|RGD:11645084|RGD:11646551|RGD:11647977|RGD:11650088|RGD:11651513|RGD:11651731|RGD:11654124|RGD:11654996|RGD:11655707|RGD:11656040|RGD:28869659|RGD:28873873|RGD:28874166|RGD:28875672|RGD:28878582|RGD:28880713|RGD:28883563|RGD:28904546|RGD:28904549|RGD:28905211 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448695|RGD:10448711|RGD:10448739|RGD:10448745|RGD:10448751|RGD:10448762 (Homo sapiens)
&
RGD:10448695|RGD:10448711|RGD:10448739|RGD:10448745|RGD:10448751|RGD:10448762 (Homo sapiens)
&
RGD:10448695|RGD:10448711|RGD:10448739|RGD:10448745|RGD:10448751|RGD:10448762 (Homo sapiens)
&
RGD:10448695|RGD:10448711|RGD:10448739|RGD:10448745|RGD:10448751|RGD:10448762 (Homo sapiens)
&
RGD:10448695|RGD:10448711|RGD:10448739|RGD:10448745|RGD:10448751|RGD:10448762 (Homo sapiens)
&
RGD:10448695|RGD:10448711|RGD:10448739|RGD:10448745|RGD:10448751|RGD:10448762 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:26092869
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:127246120|RGD:151799402 (Homo sapiens)
&
RGD:127246120|RGD:151799402 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:19777577
PMID:25741868
PMID:28492532
An association has been curated linking
CC2D2A
and
Joubert syndrome 9
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:10448730|RGD:10448794 (Homo sapiens)
&
RGD:10448730|RGD:10448794 (Homo sapiens)
8
RGD objects have been annotated to
Joubert syndrome 9
(DOID:0111004)
8
papers in RGD have been used to annotate
CC2D2A
Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 9
Original References(s):
PMID:25741868
PMID:26092869
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