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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Folate receptor alpha
Summary
- UniProt ID
- P15328
- Gene Symbol
-
- FOLR1
- FOLR
- Organism
- Homo sapiens (human)
External Links
- GlycoProtDB
- GPDB0011537
- GlyConnect
- GlyGen
- P15328
- PubChem
- P15328
- The Human Metabolome Database
- HMDBP02326
- The O-GlcNAc Database
- P15328
- RaftProt
- P15328
Annotation
- Keyword
-
- 3D-structure
- Cell membrane
- Cytoplasmic vesicle
- Direct protein sequencing
- Disulfide bond
- Endosome
- Folate-binding
- GPI-anchor
- Neurodegeneration
- Receptor
- Reference proteome
- Secreted
- Signal
- Transport
- Gene Ontology (GO)
| GO Term |
|---|
| fusion of sperm to egg plasma membrane involved in single fertilization |
| folic acid transport |
| axon regeneration |
| sperm-egg recognition |
| regulation of canonical Wnt signaling pathway |
| GO Term |
|---|
| endosome |
| endoplasmic reticulum membrane |
| external side of plasma membrane |
| cell surface |
| ER to Golgi transport vesicle membrane |
| endoplasmic reticulum-Golgi intermediate compartment membrane |
| GO Term |
|---|
| signaling receptor activity |
| folic acid receptor activity |
| folic acid binding |
Sequence
MAQRMTTQLLLLLVWVAVVGEAQTRIAWARTELLNVCMNAKHHKEKPGPEDKLHEQCRPWRKNACCSTNTSQEAHKDVSYLYRFNWNHCGEMAPACKRHFIQDTCLYECSPNLGPWIQQVDQSWRKERVLNVPLCKEDCEQWWEDCRTSYTCKSNWHKGWNWTSGFNKCAVGAACQPFHFYFPTPTVLCNEIWTHSYKVSNYSRGSGRCIQMWFDPAQGNPNEEVARFYAAAMSGAGPWAAWPFLLSLALMLLWLLS
Glycosylation Sites
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| COPI-mediated anterograde transport | Homo sapiens |
| COPII-mediated vesicle transport | Homo sapiens |
| Cargo concentration in the ER | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060644 | chondrodysplasia-pseudohermaphroditism syndrome | |
| DOID:0060764 | autosomal recessive Robinow syndrome | |
| DOID:0060765 | autosomal dominant Robinow syndrome 2 | |
| DOID:0060766 | autosomal dominant Robinow syndrome 1 | |
| DOID:0060767 | autosomal dominant Robinow syndrome 3 | |
| DOID:0080016 | spina bifida | |
| DOID:10534 | stomach cancer | |
| DOID:1089 | tethered spinal cord syndrome | |
| DOID:1138 | spinal meningioma | |
| DOID:11725 | Cornelia de Lange syndrome |
