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
folate receptor alpha
Summary
- Gene Symbol
-
- FOLR1
- Aliases
-
- FRĪ±
- Organism
- Homo sapiens (human)
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
- Proteins
| UniProt | Protein Name |
|---|---|
| P15328 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| regulation of transforming growth factor beta receptor signaling pathway | ||
| pharyngeal arch artery morphogenesis | ||
| receptor-mediated endocytosis |
|
|
| folic acid metabolic process | ||
| folic acid transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleus | ||
| ER to Golgi transport vesicle membrane |
|
|
| endoplasmic reticulum-Golgi intermediate compartment membrane |
|
|
| endosome | ||
| transport vesicle |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| folic acid receptor activity | ||
| folic acid binding | ||
| signaling receptor activity | ||
| protein binding |
GO Hierarchy
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:5844 | myocardial infarction | |
| DOID:5854 | silent myocardial infarction | |
| DOID:6114 | cerebral convexity meningioma | |
| DOID:6548 | angiomatous meningioma | |
| DOID:6683 | X-linked Aarskog syndrome | |
| DOID:684 | hepatocellular carcinoma | |
| DOID:6869 | parasagittal meningioma | |
| DOID:7210 | psammomatous meningioma | |
| DOID:7211 | fibrous meningioma | |
| DOID:7212 | meningothelial meningioma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0001249 | Intellectual disability |
| HP:0001250 | Seizure |
| HP:0002180 | Neurodegeneration |
| HP:0002376 | Developmental regression |
| Disease ID | Disease Name |
|---|---|
| OMIM:613068 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 102026741 | CHILA03837 | ||
| 105720385 | AOTNA04430 | ||
| 110195206 | PHACI03472 | ||
| 110195207 | PHACI03468 | ||
| 101054127 | SAIBB06061 | ||
| 101966601 | ICTTR04851 | ||
| 101606915 | JACJA01920 | ||
| 118299701 | SCOMX22616 | ||
| 102417105 | MYOLU08607 | ||
| 117030240 | RHIFE29567 |
