• View As List
• View As Table

GENE - TERM ANNOTATION REPORT

79 Annotations Found.

An association has been curated linking VAMP1 and Spastic paraplegia 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:151734924 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:151866107 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156047691 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:155988672 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152090895 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152032574 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152071365 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152165635 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152122704 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152114381 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152094196 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152121302 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152106458 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152041974 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152123037 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152090988 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152027962 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152118724 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152049041 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:152159778 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156023949 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:13615869 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28253535 PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:41407209 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:25741868 PMID:26467025 PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:15131239 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:26885694 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:38478442 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:11350187 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:11774073 PMID:22958904 PMID:26467025 PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156437640 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:25741868 PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:126735822 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:151847511 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:151726617 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:151753635 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:151810441 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:13478742 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:26467025 PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:151748673 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:17576681 PMID:28492532 PMID:9536098

An association has been curated linking VAMP1 and Spastic paraplegia 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:151885843 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:151836641 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:151858232 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28253535 PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:151848229 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:150548069 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:15143190 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:25741868 PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:14393082 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:25741868 PMID:28168212 PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156444627 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:151719903 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28253535 PMID:28492532 PMID:30293248

An association has been curated linking VAMP1 and Spastic paraplegia 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:155801013 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:17576681 PMID:22958904 PMID:26467025 PMID:28492532 PMID:9536098

An association has been curated linking VAMP1 and Spastic paraplegia 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:156110003 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156365315 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:155950464 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156387609 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156313771 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156116993 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156302614 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156208998 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:17576681 PMID:28492532 PMID:9536098

An association has been curated linking VAMP1 and Spastic paraplegia 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:155801005 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:26467025 PMID:28253535 PMID:28492532 PMID:33631708

An association has been curated linking VAMP1 and Spastic paraplegia 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:156163765 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:11641794 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28253535 PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:13802575 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:26467025 PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156363107 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156031744 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:150431953 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:26467025 PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156093137 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:156396229 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for human HPO-to-gene-to-disease annotations
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Original References(s): OMIM:108600

An association has been curated linking VAMP1 and Spastic paraplegia in Homo sapiens.        

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for human HPO-to-gene-to-disease annotations
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Original References(s): ORPHA:251282

An association has been curated linking VAMP1 and Spastic paraplegia 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:401830156 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:17576681 PMID:28492532 PMID:9536098

An association has been curated linking VAMP1 and Spastic paraplegia 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:405176645 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:402472558 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:405109077 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:405185778 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:405111406 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:405022525 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:405110627 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:405236490 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:405179238 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:405106696 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:405176313 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:405198845 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

An association has been curated linking VAMP1 and Spastic paraplegia 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:405110391 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532 PMID:35499206

An association has been curated linking VAMP1 and Spastic paraplegia 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:405107345 (Homo sapiens)
308 RGD objects have been annotated to Spastic paraplegia  (HP:0001258)
5 papers in RGD have been used to annotate VAMP1
Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia
Original References(s): PMID:28492532

Go Back to source page

Continue to Ontology report