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Standards Ontologies Notations
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)
Annotation information from UniProt.
Sequence
MAQRMTTQLLLLLVWVAVVGEAQTRIAWARTELLNVCMNAKHHKEKPGPEDKLHEQCRPWRKNACCSTNTSQEAHKDVSYLYRFNWNHCGEMAPACKRHFIQDTCLYECSPNLGPWIQQVDQSWRKERVLNVPLCKEDCEQWWEDCRTSYTCKSNWHKGWNWTSGFNKCAVGAACQPFHFYFPTPTVLCNEIWTHSYKVSNYSRGSGRCIQMWFDPAQGNPNEEVARFYAAAMSGAGPWAAWPFLLSLALMLLWLLS
  • N : N-glycosylation Site
  • ___ : Potential Sequon
Glycosylation Sites
Displaying all 4 entries
Position Description PubMed ID GlyTouCan ID Source
69 N-linked (GlcNAc...) asparagine
161 N-linked (GlcNAc...) asparagine
201 N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 3 entries
Pathway Name Organism
COPI-mediated anterograde transport Homo sapiens
COPII-mediated vesicle transport Homo sapiens
Cargo concentration in the ER Homo sapiens
Disease
Displaying entries 11 - 20 of 110 in total
DO ID Disease Name Source
DOID:0060581 Noonan syndrome 3
DOID:0060582 Noonan syndrome 4
DOID:0060583 Noonan syndrome 5
DOID:0060584 Noonan syndrome 6
DOID:0060585 Noonan syndrome 7
DOID:0060586 Noonan syndrome 8
DOID:0060587 Noonan syndrome 9
DOID:0060588 Noonan syndrome 10
DOID:0060608 microcephalic osteodysplastic primordial dwarfism type I
DOID:0060609 microcephalic osteodysplastic primordial dwarfism type II
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: August 19, 2024