Disease ID | Disease name | Source of annotation with PRNP | OMIM link | Number of associated genes | genes |
---|---|---|---|---|---|
123400 | CREUTZFELDT-JAKOB DISEASE | ClinVar, OMIM, HUMSAVAR | link to OMIM | 2 | PRNP, HLA-DQB1 |
137440 | GERSTMANN-STRAUSSLER DISEASE | ClinVar, OMIM, HUMSAVAR | link to OMIM | 1 | PRNP |
600072 | FATAL FAMILIAL INSOMNIA | ClinVar, OMIM, HUMSAVAR | link to OMIM | 1 | PRNP |
603218 | HUNTINGTON DISEASE-LIKE 1 | ClinVar, OMIM | link to OMIM | 1 | PRNP |
606688 | SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES | OMIM, HUMSAVAR | link to OMIM | 1 | PRNP |
245300 | KURU, SUSCEPTIBILITY TO | OMIM | link to OMIM | 1 | PRNP |
Download the gene annotation in CSV format
KEGG pathway | KEGG ID | KEGG IC |
---|---|---|
Prion diseases | hsa05020 | 7.48 |
REACTOME pathway | REACTOME ID | REACTOME IC |
---|---|---|
NCAM signaling for neurite out-growth | R-HSA-375165 | 4.9 |
Axon guidance | R-HSA-422475 | 3.93 |
NCAM1 interactions | R-HSA-419037 | 7.59 |
Developmental Biology | R-HSA-1266738 | 3.48 |
GO term | GO ID | GO IC |
---|---|---|
cation binding | GO:0043169 | 1.4 |
tubulin binding | GO:0015631 | 4.1 |
metal ion binding | GO:0046872 | 1.41 |
transition metal ion binding | GO:0046914 | 2.48 |
cytoskeletal protein binding | GO:0008092 | 3.02 |
microtubule binding | GO:0008017 | 4.42 |
chaperone binding | GO:0051087 | 5.34 |
ion binding | GO:0043167 | 1.36 |
binding | GO:0005488 | 0.18 |
protein binding | GO:0005515 | 0.46 |
ATP-dependent protein binding | GO:0043008 | 7.66 |
ion channel binding | GO:0044325 | 5.02 |
copper ion binding | GO:0005507 | 5.71 |
identical protein binding | GO:0042802 | 2.63 |
lamin binding | GO:0005521 | 6.91 |