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GENE - TERM ANNOTATION REPORT

67 Annotations Found.

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:12913365 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:28492532 PMID:29655203

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:34890573 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:24440240 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: CTD Direct Evidence: marker/mechanism
Original References(s): PMID:15651030

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:10050613 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:25741868 PMID:26003046 PMID:26319512 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from OMIM Disease Annotation Pipeline
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:9692966 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:24415674 PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:10396040 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:26319512 PMID:26467025 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:15108623 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:21140503 PMID:25741868

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:13807036 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:21140503 PMID:24415674 PMID:25741868 PMID:28492532 PMID:29506905

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:329952065 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:23234264 PMID:31130284

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:13820057 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:19027335 PMID:19388150 PMID:24071436 PMID:24415674 PMID:25741868 PMID:28492532 PMID:35588794

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:329350819 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:23846910

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:25321420 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15651030 PMID:23234264 PMID:23660394 PMID:24415674 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:13518016 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:11136556 PMID:11978605 PMID:12557293 PMID:15108290 PMID:25741868 PMID:28438604 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:11664835 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:23660394 PMID:24268530 PMID:24415674 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:26888648 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:16855203 PMID:17171576 PMID:19027335 PMID:23660394 PMID:24268530 PMID:25741868 PMID:28492532 PMID:32214227

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:8560431 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:17101918 PMID:24415674 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:8560430 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15651030 PMID:23234264 PMID:23660394 PMID:24415674 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:150530839 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:25741868 PMID:34389248

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:10396034 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: GAMT-related condition
Original References(s): PMID:15108290 PMID:16169544 PMID:17171576 PMID:19027335 PMID:23583224 PMID:23660394 PMID:24071436 PMID:24268530 PMID:25741868 PMID:28492532 PMID:34389248

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:8566758 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:11978605 PMID:15108290 PMID:20301745 PMID:25741868

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:8566757 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:16855203 PMID:20301745 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:8566759 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:11978605 PMID:12468279 PMID:20301745 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:8560429 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:15651030 PMID:16855203 PMID:17336114 PMID:19027335 PMID:20301745 PMID:21140503 PMID:23031365 PMID:24268530 PMID:25741868 PMID:27233226 PMID:28055022 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:10396031 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:23660394 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:26923625 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:19027335 PMID:23660394 PMID:24415674 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:12907290 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:17171576 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:151236210 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:23846910 PMID:25741868 PMID:33996490

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:8560428 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:19027335 PMID:23234264 PMID:23660394 PMID:24071436 PMID:24268530 PMID:24276113 PMID:25741868 PMID:28492532 PMID:29506905 PMID:8651275

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:13626794 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:19892372 PMID:24415674 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:38462420 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:26319512 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:8566756 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:11978605 PMID:16855203 PMID:17171576 PMID:17576681 PMID:19027335 PMID:20301745 PMID:22019491 PMID:23660394 PMID:24268530 PMID:24415674 PMID:2476685 PMID:25741868 PMID:28492532 PMID:29506905 PMID:8651275 PMID:9386672 PMID:9536098

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:10397553 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:19288536 PMID:23234264 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:10396030 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:24415674 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:10397555 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:15651030 PMID:17336114 PMID:21140503 PMID:25741868 PMID:28492532 PMID:29655203

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:13211524 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:19027335 PMID:23583224 PMID:23660394 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency in Homo sapiens.        

The association was inferred from sequence or structural similarity (ISS)
The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
The annotation has been inferred from sequence or structural similarity with Gamt (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: OMIM:612736

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens) & RGD:10396023|RGD:10396028|RGD:10396037|RGD:10396038|RGD:10396039|RGD:10396041|RGD:10396044|RGD:10397552|RGD:10397557|RGD:10397558|RGD:11640347|RGD:11644125|RGD:11664777|RGD:11664791|RGD:11664793|RGD:11664819|RGD:126738510|RGD:127278160|RGD:127285972|RGD:12841410|RGD:13212280|RGD:13466731|RGD:13489548|RGD:13527510|RGD:13626789|RGD:13626793|RGD:13626797|RGD:13626798|RGD:13626800|RGD:13805754|RGD:13812292|RGD:13814035|RGD:13817411|RGD:14712453|RGD:14718517|RGD:14721133|RGD:14724941|RGD:14740139|RGD:14741802|RGD:15155164|RGD:15160910|RGD:151892006|RGD:156442672|RGD:26884857|RGD:26922336|RGD:28906345|RGD:38457186|RGD:38457895|RGD:38465652|RGD:38491974|RGD:38492636|RGD:38493421|RGD:38494181|RGD:8691176|RGD:8691177 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens) & RGD:11664837|RGD:126743162|RGD:127261069|RGD:12834907|RGD:12842663|RGD:14398987|RGD:150338737|RGD:150530840|RGD:243052146|RGD:28897821|RGD:329350820|RGD:401722262|RGD:401941313|RGD:401942857|RGD:401943806 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2 | ClinVar Annotator: match by term: GAMT-related condition
Original References(s): PMID:25741868

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:13829281 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15651030 PMID:16855203 PMID:17336114 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:156381354 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:24415674 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:14703480 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: GAMT-related condition
Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:405281809 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:25741913

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens) & RGD:10396021|RGD:10396026|RGD:10396029|RGD:10396033|RGD:11664817|RGD:126766733|RGD:126770237|RGD:126770878|RGD:12837941|RGD:13462357|RGD:13476945|RGD:13498044|RGD:13501318|RGD:13504414|RGD:13626790|RGD:13626791|RGD:13626792|RGD:13829470|RGD:14701757|RGD:15126980|RGD:15143581|RGD:151877881|RGD:8659630|RGD:8691178|RGD:8691179 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2 | ClinVar Annotator: match by term: GAMT-related condition
Original References(s): PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:151714563 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:25741868 PMID:27650626 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:156442062 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: GAMT-related condition
Original References(s): PMID:15108290 PMID:25741868 PMID:28492532 PMID:31222513

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:127268713 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:23234264 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:151760417 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:23234264 PMID:24415674 PMID:25741868 PMID:28492532 PMID:31130284

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:13816917|RGD:151769737|RGD:26886198|RGD:38483256 (Homo sapiens) & RGD:13816917|RGD:151769737|RGD:26886198|RGD:38483256 (Homo sapiens) & RGD:13816917|RGD:151769737|RGD:26886198|RGD:38483256 (Homo sapiens) & RGD:13816917|RGD:151769737|RGD:26886198|RGD:38483256 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:17576681 PMID:28492532 PMID:9536098

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:13475830 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:25741868 PMID:26003046 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:127261070 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:34015165 PMID:9536098

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:10396043 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:24415674 PMID:25741868 PMID:26003046 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens) & RGD:10056682|RGD:10397556|RGD:11664814|RGD:11665615|RGD:11665953|RGD:11665999|RGD:11666387|RGD:14725681|RGD:150338536|RGD:156438336|RGD:28897549|RGD:28897553|RGD:28897555|RGD:28897557|RGD:28906981|RGD:28906983|RGD:329350816|RGD:329350846|RGD:329846813|RGD:401722261|RGD:401722265|RGD:401722267|RGD:401962024|RGD:401962025|RGD:40905372|RGD:8691180|RGD:8692231 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:40815153 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:23234264 PMID:25741868 PMID:28492532 PMID:31130284

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:151715985|RGD:38482596 (Homo sapiens) & RGD:151715985|RGD:38482596 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:19027335 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:10396032|RGD:10396046|RGD:13211751 (Homo sapiens) & RGD:10396032|RGD:10396046|RGD:13211751 (Homo sapiens) & RGD:10396032|RGD:10396046|RGD:13211751 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2 | ClinVar Annotator: match by term: GAMT-related condition
Original References(s): PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:127255229 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:19288536 PMID:23234264 PMID:25741868 PMID:28492532 PMID:31130284

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:10396042|RGD:11664775 (Homo sapiens) & RGD:10396042|RGD:11664775 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:26467025 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:127239398|RGD:127257550|RGD:127263690|RGD:12848890|RGD:151888548|RGD:155267417|RGD:156347750|RGD:26912635|RGD:26913655|RGD:26920413|RGD:38487841|RGD:401941314 (Homo sapiens) & RGD:127239398|RGD:127257550|RGD:127263690|RGD:12848890|RGD:151888548|RGD:155267417|RGD:156347750|RGD:26912635|RGD:26913655|RGD:26920413|RGD:38487841|RGD:401941314 (Homo sapiens) & RGD:127239398|RGD:127257550|RGD:127263690|RGD:12848890|RGD:151888548|RGD:155267417|RGD:156347750|RGD:26912635|RGD:26913655|RGD:26920413|RGD:38487841|RGD:401941314 (Homo sapiens) & RGD:127239398|RGD:127257550|RGD:127263690|RGD:12848890|RGD:151888548|RGD:155267417|RGD:156347750|RGD:26912635|RGD:26913655|RGD:26920413|RGD:38487841|RGD:401941314 (Homo sapiens) & RGD:127239398|RGD:127257550|RGD:127263690|RGD:12848890|RGD:151888548|RGD:155267417|RGD:156347750|RGD:26912635|RGD:26913655|RGD:26920413|RGD:38487841|RGD:401941314 (Homo sapiens) & RGD:127239398|RGD:127257550|RGD:127263690|RGD:12848890|RGD:151888548|RGD:155267417|RGD:156347750|RGD:26912635|RGD:26913655|RGD:26920413|RGD:38487841|RGD:401941314 (Homo sapiens) & RGD:127239398|RGD:127257550|RGD:127263690|RGD:12848890|RGD:151888548|RGD:155267417|RGD:156347750|RGD:26912635|RGD:26913655|RGD:26920413|RGD:38487841|RGD:401941314 (Homo sapiens) & RGD:127239398|RGD:127257550|RGD:127263690|RGD:12848890|RGD:151888548|RGD:155267417|RGD:156347750|RGD:26912635|RGD:26913655|RGD:26920413|RGD:38487841|RGD:401941314 (Homo sapiens) & RGD:127239398|RGD:127257550|RGD:127263690|RGD:12848890|RGD:151888548|RGD:155267417|RGD:156347750|RGD:26912635|RGD:26913655|RGD:26920413|RGD:38487841|RGD:401941314 (Homo sapiens) & RGD:127239398|RGD:127257550|RGD:127263690|RGD:12848890|RGD:151888548|RGD:155267417|RGD:156347750|RGD:26912635|RGD:26913655|RGD:26920413|RGD:38487841|RGD:401941314 (Homo sapiens) & RGD:127239398|RGD:127257550|RGD:127263690|RGD:12848890|RGD:151888548|RGD:155267417|RGD:156347750|RGD:26912635|RGD:26913655|RGD:26920413|RGD:38487841|RGD:401941314 (Homo sapiens) & RGD:127239398|RGD:127257550|RGD:127263690|RGD:12848890|RGD:151888548|RGD:155267417|RGD:156347750|RGD:26912635|RGD:26913655|RGD:26920413|RGD:38487841|RGD:401941314 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2 | ClinVar Annotator: match by term: GAMT-related condition
Original References(s): PMID:15108290 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:11350362|RGD:38492576 (Homo sapiens) & RGD:11350362|RGD:38492576 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:26003046 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:13626788|RGD:329350818 (Homo sapiens) & RGD:13626788|RGD:329350818 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:24415674 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:21070248 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:16054853 PMID:16855203 PMID:21140503 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:151353260|RGD:329350817 (Homo sapiens) & RGD:151353260|RGD:329350817 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:24415674

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:14712862|RGD:26919533 (Homo sapiens) & RGD:14712862|RGD:26919533 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:16199547 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:401962027 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:23660394 PMID:24071436 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:127247363|RGD:26895606|RGD:26915808|RGD:38596594 (Homo sapiens) & RGD:127247363|RGD:26895606|RGD:26915808|RGD:38596594 (Homo sapiens) & RGD:127247363|RGD:26895606|RGD:26915808|RGD:38596594 (Homo sapiens) & RGD:127247363|RGD:26895606|RGD:26915808|RGD:38596594 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2
Original References(s): PMID:15108290 PMID:16199547 PMID:25741868 PMID:28492532

An association has been curated linking GAMT and guanidinoacetate methyltransferase deficiency 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:329350814|RGD:329350821 (Homo sapiens) & RGD:329350814|RGD:329350821 (Homo sapiens)
3 RGD objects have been annotated to guanidinoacetate methyltransferase deficiency  (DOID:0050799)
13 papers in RGD have been used to annotate GAMT
Curation Notes: ClinVar Annotator: match by term: CEREBRAL CREATINE DEFICIENCY SYNDROME 2 | ClinVar Annotator: match by term: GAMT-related condition
Original References(s): PMID:24415674 PMID:25741868

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