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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
phosphoribosyl pyrophosphate synthetase 1
Summary
- Gene Symbol
-
- PRPS1
- Aliases
-
- CMTX5
- DFNX1
- PPRibP
- PRS I
- PRS-I
- ribose-phosphate diphosphokinase 1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- ATP-binding
- Alternative splicing
- Charcot-Marie-Tooth disease
- Direct protein sequencing
- Disease variant
- Gout
- Intellectual disability
- Kinase
- Magnesium
- Metal-binding
- Neurodegeneration
- Non-syndromic deafness
- Nucleotide biosynthesis
- Reference proteome
- Retinitis pigmentosa
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| purine nucleotide biosynthetic process | ||
| urate biosynthetic process | ||
| pyrimidine nucleotide biosynthetic process |
|
GO Hierarchy
biological process
metabolic process [inference]
nitrogen compound metabolic process [inference]
biosynthetic process [inference]
cellular metabolic process [inference]
cellular aromatic compound metabolic process [inference]
phosphorus metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
cellular biosynthetic process [inference]
heterocycle metabolic process [inference]
primary metabolic process [inference]
small molecule metabolic process [inference]
organic substance metabolic process [inference]
cellular process [inference]
cellular metabolic process [inference]
cellular aromatic compound metabolic process [inference]
phosphorus metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
cellular biosynthetic process [inference]
heterocycle metabolic process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| ribose phosphate diphosphokinase complex | ||
| cytosol |
|
|
| cytoplasm |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| kinase activity | ||
| magnesium ion binding | ||
| protein homodimerization activity | ||
| ATP binding | ||
| protein binding |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:26 | pancreas disease | |
| DOID:10003 | sensorineural hearing loss | |
| DOID:10554 | meningoencephalitis | |
| DOID:10584 | retinitis pigmentosa | |
| DOID:1059 | intellectual disability | |
| DOID:10595 | Charcot-Marie-Tooth disease | |
| DOID:1074 | kidney failure | |
| DOID:1142 | alternating exotropia | |
| DOID:1143 | exotropia | |
| DOID:11771 | spontaneous ocular nystagmus |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000028 | Cryptorchidism |
| HP:0000047 | Hypospadias |
| HP:0000083 | Renal insufficiency |
| HP:0000154 | Wide mouth |
| HP:0000218 | High palate |
| HP:0000268 | Dolichocephaly |
| HP:0000286 | Epicanthus |
| HP:0000316 | Hypertelorism |
| HP:0000325 | Triangular face |
| HP:0000365 | Hearing impairment |
| Disease ID | Disease Name |
|---|---|
| ORPHA:423479 |
|
| OMIM:311070 |
|
| ORPHA:411543 |
|
| OMIM:301835 |
|
| OMIM:304500 |
|
| ORPHA:1187 |
|
| ORPHA:411536 |
|
| OMIM:300661 |
|
| ORPHA:99014 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 481011 | CANLF20037 | ||
| 112932027 | VULVU27702 | ||
| 100465510 | AILME09389 | ||
| 101674476 | MUSPF06267 | ||
| 101086044 | FELCA38674 | ||
| 123378925 | FELCA38674 | ||
| 101322320 | TURTR03994 | ||
| 118888926 | BALMU19547 | ||
| 100054730 | HORSE44480 | ||
| 100517744 | PIGXX37823 |
