TF

Gene Information
 
Gene Symbol
TF
 
Aliases
HEL-S-71p, PRO1557, PRO2086, TFQTL1
 
Entrez Gene ID
 
Gene Name
Transferrin
 
Chromosomal Location
3q22.1
 
HGNC ID
 
Summary
This gene encodes a glycoprotein with an approximate molecular weight of 76.5 kDa. It is thought to have been created as a result of an ancient gene duplication event that led to generation of homologous C and N-terminal domains each of which binds one ion of ferric iron. The function of this protein is to transport iron from the intestine, reticuloendothelial system, and liver parenchymal cells to all proliferating cells in the body. This protein may also have a physiologic role as granulocyte/pollen-binding protein (GPBP) involved in the removal of certain organic matter and allergens from serum. [provided by RefSeq, Sep 2009]
 
RefSeq DNA
 
RefSeq mRNA
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0001895 Biological process Retina homeostasis HEP 23580065
GO:0031647 Biological process Regulation of protein stability TAS 25635054
GO:0034756 Biological process Regulation of iron ion transport IGI 18353247
GO:0048260 Biological process Positive regulation of receptor-mediated endocytosis IDA 12704209
GO:0048260 Biological process Positive regulation of receptor-mediated endocytosis IGI 18353247
Protein Information
 
Protein Name
Serotransferrin, beta-1 metal-binding globulin, epididymis secretory sperm binding protein Li 71p, siderophilin
 
Function
Transferrins are iron binding transport proteins which can bind two Fe(3+) ions in association with the binding of an anion, usually bicarbonate. It is responsible for the transport of iron from sites of absorption and heme degradation to those of storage and utilization. Serum transferrin may also have a further role in stimulating cell proliferation
 
Refseq Proteins
 
UniProt
 
PDB
 
Pfam
Pfam Accession Pfam ID
PF00405 Transferrin
Pathways
 
KEGG
 
Reactome
 

HIF-1 signaling pathway
Ferroptosis
Mineral absorption

 

Platelet degranulation
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
Cargo recognition for clathrin-mediated endocytosis
Clathrin-mediated endocytosis
Post-translational protein phosphorylation
Iron uptake and transport
Transferrin endocytosis and recycling

Interactions
 
STRING MINT IntAct
ENSP00000155840 P51787 P51787
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Blood Disorders
Anemia
Digestive System Diseases
Fatty Liver
Liver Diseases
Hepatitis
Endocrine System Diseases
PCOS
References
 
 
PubMed ID Associated gene/s Associated condition Genetic Mutation Diagnostic Criteria Association with PCOS Ethnicity Conclusion
CK-9, A1AT, CK-1, APOA-1, ATTR, DBP, HP, DRAM2, APOA-4, IL12-A, SIRT2, FGG, FGB, ZAG, RBP, A1BG, GLUT4, SERPINA1, SPTLC2, MAK 
PCOS, increased risk of insulin resistance, abnormal glucose metabolism, type II diabetes, abnormal lipid metabolism, hyperinsulinemia 
 
Rotterdam consensus criteria 
Related 
30 PCOS and 30 normal 
Thirty-two protein spots were shown to be significantly differentially expressed between PCOS and normal follicular fluids, of which 20 unique proteins were identified to be associated with cellular metabolism and physiological processes; 13 of these proteins were upregulated while seven were downregulated in PCOS follicular fluids. Semiquantitative reverse transcription-polymerase chain reaction (RTPCR) analyses revealed that mRNA levels of serine palmitoyltransferase 2, serine/threonine-protein kinase male germ cell-associated kinase (MAK) and DNA damage-regulated autophagy modulator protein 2 decreased significantly in granulosa cells of PCOS patients compared with normal samples. 

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