Version: 8.0.0
Date: Tue Jan 28 2025
Home
Data and Tools
Downloads
API
AllianceMine
JBrowse 2
Submit Data
Textpresso
Tools and Prototypes
Members
FlyBase
Mouse Genome Database
Rat Genome Database
Saccharomyces Genome Database
WormBase
Xenbase
Zebrafish Information Network
Gene Ontology Consortium
News
News and Events
Release Notes
Event Calendar
About
About Us
Funding
Publications
Organization and Governance
Privacy, Warranty, Licensing, and Data Preservation Commitment
Help
FAQ / Known Issues
Glossary
Tutorials
User Documentation
Community
Alliance User Community
Facebook
Mastodon
Bluesky
Github
Contact Us
Cite Us
All
All
Gene
Gene Ontology
Disease
Allele/Variant
Model
HTP Dataset Index
Disease
Show all Categories
Disease Group
sensory system disease
2
×
monogenic disease
1
×
Genes
PRP31 (Sce)
2
×
PRPF31 (Hsa)
2
×
Prp31 (Dme)
2
×
Prpf31 (Mmu)
2
×
Prpf31 (Rno)
2
×
Show More
Associated Species
Caenorhabditis elegans
2
×
Danio rerio
2
×
Drosophila melanogaster
2
×
Homo sapiens
2
×
Mus musculus
2
×
Rattus norvegicus
2
×
Saccharomyces cerevisiae
2
×
Xenopus laevis
2
×
Xenopus tropicalis
2
×
Show More
Filter
2
results
Page 1 of 1
Disease
Genes: Prpf31 (Rno)
retinitis pigmentosa
Disease
Source:
DOID:10584
Definition:
A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss.
Genes:
Prpf31 (Rno)
Gene (965)
Allele/Variant (119)
Model (104)
retinitis pigmentosa 11
Disease
Source:
DOID:0110408
Definition:
A retinitis pigmentosa that has_material_basis_in mutation in the PRPF31 gene on chromosome 19q13.
Genes:
Prpf31 (Rno)
Gene (10)
Allele/Variant (5)
Model (1)
Page 1 of 1
You need to enable JavaScript to run this app.