Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
ADP-ribosylhydrolase ARH3
Summary
- UniProt ID
- Q9NX46
- Gene Symbol
-
- ADPRS
- ADPRHL2
- ARH3
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- Q9NX46
- PubChem
- Q9NX46
- The Human Metabolome Database
- HMDBP02546
- The O-GlcNAc Database
- Q9NX46
Annotation
- Keyword
-
- 3D-structure
- Chromosome
- Cytoplasm
- DNA repair
- Disease variant
- Hydrolase
- Magnesium
- Metal-binding
- Mitochondrion
- Neurodegeneration
- Nucleus
- Phosphoprotein
- Reference proteome
- Gene Ontology (GO)
| GO Term |
|---|
| nucleus |
| cytoplasm |
| mitochondrion |
| mitochondrial matrix |
| nucleoplasm |
| nuclear body |
| site of DNA damage |
Sequence
MAAAAMAAAAGGGAGAARSLSRFRGCLAGALLGDCVGSFYEAHDTVDLTSVLRHVQSLEPDPGTPGSERTEALYYTDDTAMARALVQSLLAKEAFDEVDMAHRFAQEYKKDPDRGYGAGVVTVFKKLLNPKCRDVFEPARAQFNGKGSYGNGGAMRVAGISLAYSSVQDVQKFARLSAQLTHASSLGYNGAILQALAVHLALQGESSSEHFLKQLLGHMEDLEGDAQSVLDARELGMEERPYSSRLKKIGELLDQASVTREEVVSELGNGIAAFESVPTAIYCFLRCMEPDPEIPSAFNSLQRTLIYSISLGGDTDTIATMAGAIAGAYYGMDQVPESWQQSCEGYEETDILAQSLHRVFQKS
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
|
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| POLB-Dependent Long Patch Base Excision Repair | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060260 | ptosis | |
| DOID:0060261 | congenital ptosis | |
| DOID:0090105 | autosomal recessive hypercholesterolemia | |
| DOID:10127 | cerebral artery occlusion | |
| DOID:1059 | intellectual disability | |
| DOID:11771 | spontaneous ocular nystagmus | |
| DOID:11832 | visual epilepsy | |
| DOID:1289 | neurodegenerative disease | |
| DOID:13174 | dissociated nystagmus | |
| DOID:1443 | cerebral degeneration |
