FOLR3 - folate receptor gamma Gene
Also Known as FR-G; FRgamma; FR-gamma; gamma-hFR
Species: Homo sapiens
About FOLR3
This gene has 5 transcripts (splice variants), 213 orthologues and 4 paralogues. Biased expression in bone marrow (RPKM 27.0), appendix (RPKM 4.9) and 3 other tissues.
Summary
This gene encodes a member of the folate receptor (FOLR) family of proteins, which have a high affinity for folic acid and for several reduced folic acid derivatives, and mediate delivery of 5-methyltetrahydrofolate to the interior of cells. Expression of this gene may be elevated in ovarian and primary peritoneal carcinoma. This gene is present in a gene cluster on chromosome 11. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]
FOLR3 Products (2)
| mRNA | Protein | Name |
|---|---|---|
| NM_000804.4 | NP_000795.2 | folate receptor gamma isoform 1 precursor |
| NM_001412270.1 | NP_001399199.1 | folate receptor gamma isoform 2 precursor |
| Molecular Function GO Annotation | Evidence | Verweise | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
32296183 | GOA |
FOLR3 Protein Structure
Folate_rec: Folate receptor family (146 - 253)
- 0
- 100
- 200
- 287 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
folate receptor gamma |
|
FOLR3 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | Verweise |
|---|---|---|---|---|---|---|---|
|
Intra
|
FOLR3 | P41439 | ANKRD11 | Homo sapiens | X5D778 | 32296183 | |
|
Intra
|
FOLR3 | P41439 | UBQLN1 | Homo sapiens | Q9UMX0 | 32296183 |
Recombinant FOLR3 Proteins
| Art. -Nr. | Produktname | Accession | Reinheit |
|---|---|---|---|
| HY-P78766 | FOLR3 Protein, Human (HEK293, His) | P41439 (Q23-S245) | ≥ 95%, as determined by reducing SDS-PAGE. |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Primary Peritoneal Carcinoma |
|
|
| Choriocarcinoma Of The Testis |
|
|
| Subacute Leukemia |
|
|
| Folate Malabsorption, Hereditary |
|
|
| Exudative Vitreoretinopathy 3 |
|
|
| Neural Tube Defects |
|
|