Welcome
{{ username}}
Message Center
{{ messageCount }} Messages
Go to Message Center
Watched Genes
{{$index + 1}}.
{{ watchedObject.symbol }} (RGD ID:{{watchedObject.rgdId}})
Modify Subscription
Unsubscribe
Watched Ontology Terms
{{$index + 1}}.
{{ watchedTerm.term }} ({{watchedTerm.accId}})
Modify Subscription
Unsubscribe
{{gene.symbol}}:
{{ gene.description }}
×
Save List to My RGD
Create Name:
Description:
You must be logged in to use this feature
{{ loginError }}
{{ watchLinkText }}
Select categories you would like to watch. Updates to this gene will be sent to {{ username }}
{{geneWatchAttr}}
Analyze
Gene
Strain
QTL
List
×
Gene Annotator (Functional Annotation)
unavailable
Gene Annotator (Annotation Distribution)
unavailable
Variant Visualizer (Genomic Variants)
unavailble
Variant Visualizer (Genomic Variants)
unavailable
Gene Annotator (Functional Annotation)
Gene Annotator (Annotation Distribution)
Variant Visualizer (Genomic Variants)
InterViewer (Protein-Protein Interactions)
unavailable
Gviewer (Genome Viewer)
unavailable
Variant Visualizer (Damaging Variants) unavailble
Variant Visualizer (Damaging Variants)
unavailable
InterViewer (Protein-Protein Interactions)
GViewer (Genome Viewer)
Variant Visualizer (Damaging Variants)
Gene Annotator (Annotation Comparison)
unavailable
OLGA (Gene List Generator)
unavailable
Gene Annotator (Annotation Comparison)
OLGA (Gene List Generator)
Excel (Download)
MOET (Multi-Ontology Enrichement)
unavailable
GOLF (Gene-Ortholog Location Finder)
unavailable
MOET (Multi-Ontology Enrichement)
GOLF (Gene-Ortholog Location Finder)
x
Send Message
x
Send us a Message
Your email
Message
Send
Submit Data
|
Help
|
Video Tutorials
|
News
|
Publications
|
Download
|
REST API
|
Citing RGD
|
Contact
Home
Search RGD
Grant Resources
Citing RGD
About Us
Contact Us
Data
Genes
Variants
Community Projects
QTLs
Strains
Markers
Genome Information
Ontologies
Cell Lines
References
Download
Submit Data
Analysis & Visualization
OntoMate (Literature Search)
JBrowse (Genome Browser)
Synteny Browser (VCMap)
Variant Visualizer
Multi-Ontology Enrichment (MOET)
Gene-Ortholog Location Finder (GOLF)
InterViewer (Protein-Protein Interactions)
PhenoMiner (Quatitative Phenotypes)
Gene Annotator
OLGA (Gene List Generator)
AllianceMine
GViewer (Genome Viewer)
Diseases
Aging & Age-Related Disease
Cancer & Neoplastic Disease
Cardiovascular Disease
Coronavirus Disease
Developmental Disease
Diabetes
Hematologic Disease
Immune & Inflammatory Disease
Infectious Disease
Liver Disease
Neurological Disease
Obesity & Metabolic Syndrome
Renal Disease
Respiratory Disease
Sensory Organ Disease
Phenotypes & Models
Find Models
new
Genetic Models
Autism Models
Rat PhenoMiner (Quantitative Phenotypes)
Chinchilla PhenoMiner
Expected Ranges (Quantitative Phenotype)
PhenoMiner Term Comparison
Hybrid Rat Diversity Panel
Phenotypes
Phenotypes in Other Animal Models
Animal Husbandry
Strain Medical Records
Phylogenetics
Strain Availability
Calendar
Rats 101
Submissions
Photo Archive
Pathways
Community
Rat Community Forum
Directory of Rat Laboratories
Video Tutorials
News
RGD Publications
RGD Presentations Archive
Nomenclature Guidelines
Resource Links
Laboratory Resources
Employment Resources
Advanced Search (OLGA)
View As List
View As Table
GENE - TERM ANNOTATION REPORT
2 Annotations Found.
An association has been curated linking
ALPL
and
childhood hypophosphatasia
in Sus scrofa.
The association was
inferred from sequence orthology
(ISO)
The annotation was made from
OMIM Disease Annotation Pipeline
The annotation has been inferred from sequence orthology with
ALPL (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
1
RGD objects have been annotated to
childhood hypophosphatasia
(DOID:0110915)
0
papers in RGD have been used to annotate
ALPL
An association has been curated linking
ALPL
and
childhood hypophosphatasia
in Sus scrofa.
The association was
inferred from sequence orthology
(ISO)
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 from sequence orthology with
ALPL (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
1
RGD objects have been annotated to
childhood hypophosphatasia
(DOID:0110915)
0
papers in RGD have been used to annotate
ALPL
Curation Notes: ClinVar Annotator: match by term: Childhood hypophosphatasia
Original References(s):
PMID:10094560
PMID:10332035
PMID:10508980
PMID:10636450
PMID:10679946
PMID:10839996
PMID:10872988
PMID:11438998
PMID:11479741
PMID:11760847
PMID:11855933
PMID:12162492
PMID:12357339
PMID:12412800
PMID:12638946
PMID:12815606
PMID:12920074
PMID:1409720
PMID:15135428
PMID:15137467
PMID:15660230
PMID:15671102
PMID:15694177
PMID:16583935
PMID:17213282
PMID:17229666
PMID:17253930
PMID:17719863
PMID:17916236
PMID:17922851
PMID:18340466
PMID:18455459
PMID:18559907
PMID:18769927
PMID:19232125
PMID:19335222
PMID:19500388
PMID:20089612
PMID:20739387
PMID:21168482
PMID:21228398
PMID:21713987
PMID:21956185
PMID:22397652
PMID:22781519
PMID:22913777
PMID:22995991
PMID:24022022
PMID:24033266
PMID:24276437
PMID:24378058
PMID:24569605
PMID:25023282
PMID:25716980
PMID:25731960
PMID:25736332
PMID:25741868
PMID:26272126
PMID:26432670
PMID:26467025
PMID:26783040
PMID:27179278
PMID:27507156
PMID:27884173
PMID:27920814
PMID:28127875
PMID:28401263
PMID:28436937
PMID:28492530
PMID:28492532
PMID:28506345
PMID:28580391
PMID:28663156
PMID:28749478
PMID:28763161
PMID:28881669
PMID:29236161
PMID:29724887
PMID:30249491
PMID:30283912
PMID:30576866
PMID:30719581
PMID:30979366
PMID:31077853
PMID:31088113
PMID:31641588
PMID:31707452
PMID:3174660
PMID:32160374
PMID:32803091
PMID:32973344
PMID:33549410
PMID:33814268
PMID:33977024
PMID:34000433
PMID:34213743
PMID:34515659
PMID:34627339
PMID:34662886
PMID:34712267
PMID:36444396
PMID:7833929
PMID:8406453
PMID:8675582
PMID:8954059
PMID:9452105
PMID:9618260
PMID:9781036
PMID:9814472
Go Back to source page
Continue to Ontology report