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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Phosphatidylinositol polyphosphate 5-phosphatase type IV
Summary
- UniProt ID
- Q9NRR6
- Gene Symbol
-
- INPP5E
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- Q9NRR6
- PubChem
- Q9NRR6
- SwissLipids
- The Human Metabolome Database
- HMDBP01572
- The O-GlcNAc Database
- Q9NRR6
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Cilium
- Cytoskeleton
- Disease variant
- Golgi apparatus
- Hydrolase
- Intellectual disability
- Joubert syndrome
- Lipid metabolism
- Methylation
- Nucleus
- Obesity
- Phosphoprotein
- Prenylation
- Reference proteome
- Repeat
- Gene Ontology (GO)
| GO Term |
|---|
| Golgi membrane |
| nucleus |
| Golgi apparatus |
| plasma membrane |
| cilium |
| axoneme |
| cytosol |
| ruffle |
| Golgi cisterna membrane |
Sequence
MPSKAENLRPSEPAPQPPEGRTLQGQLPGAPPAQRAGSPPDAPGSESPALACSTPATPSGEDPPARAAPIAPRPPARPRLERALSLDDKGWRRRRFRGSQEDLEARNGTSPSRGSVQSEGPGAPAHSCSPPCLSTSLQEIPKSRGVLSSERGSPSSGGNPLSGVASSSPNLPHRDAAVAGSSPRLPSLLPPRPPPALSLDIASDSLRTANKVDSDLADYKLRAQPLLVRAHSSLGPGRPRSPLACDDCSLRSAKSSFSLLAPIRSKDVRSRSYLEGSLLASGALLGADELARYFPDRNVALFVATWNMQGQKELPPSLDEFLLPAEADYAQDLYVIGVQEGCSDRREWETRLQETLGPHYVLLSSAAHGVLYMSLFIRRDLIWFCSEVECSTVTTRIVSQIKTKGALGISFTFFGTSFLFITSHFTSGDGKVAERLLDYTRTVQALVLPRNVPDTNPYRSSAADVTTRFDEVFWFGDFNFRLSGGRTVVDALLCQGLVVDVPALLQHDQLIREMRKGSIFKGFQEPDIHFLPSYKFDIGKDTYDSTSKQRTPSYTDRVLYRSRHKGDICPVSYSSCPGIKTSDHRPVYGLFRVKVRPGRDNIPLAAGKFDRELYLLGIKRRISKEIQRQQALQSQNSSTICSVS
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
|
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| ARL13B-mediated ciliary trafficking of INPP5E | Homo sapiens |
| Synthesis of PIPs at the Golgi membrane | 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:0050144 | Kartagener syndrome | |
| DOID:0050657 | Bannayan-Riley-Ruvalcaba syndrome | |
| DOID:0050777 | Joubert syndrome | |
| DOID:0050778 | Meckel syndrome | |
| DOID:0050902 | medulloblastoma | |
| DOID:0060216 | Cogan syndrome | |
| DOID:0060249 | scoliosis | |
| DOID:0060260 | ptosis | |
| DOID:0060261 | congenital ptosis | |
| DOID:0060320 | inguinal hernia |
